202 Jobs in Anupgarh - Page 5

Description Medical Scientist Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner. Attends at Trusted Process meetings and may participate in internal and external audits. Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. Qualifications Degree in life sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific experience and/or training discipline. Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential. A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work. Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership. Understanding of scientific principles to assure effective and high-quality medical data analysis. Excellent written and oral communication skills. Excellent computer skills: MS Office programs, spread sheets, presentations. Prefer knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines. Strong team player with excellent interpersonal skills and ability to work effective in a cross-functional team environment. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Show more Show less

Description Medical Scientist - Shanghai/Beijing Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner. Attends at Trusted Process meetings and may participate in internal and external audits. Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. Qualifications Degree in life sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific experience and/or training discipline. Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential. A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work. Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership. Understanding of scientific principles to assure effective and high-quality medical data analysis. Excellent written and oral communication skills. Excellent computer skills: MS Office programs, spread sheets, presentations. Prefer knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines. Strong team player with excellent interpersonal skills and ability to work effective in a cross-functional team environment. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Show more Show less

Description Safety & PV Specialist II Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Enters information into PVG quality and tracking systems for receipt and tracking ICSR as required. May assist in the preparation of the project plans such as Safety Management Plan. May perform set-up, delivery and close-out of safety and pharmacovigilance projects. ProcessesICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications and tests. Compiles complete narrative summaries. Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Participates in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements. Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases. Maintains safety tracking for assigned activities. Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, and MedDRA coding as required. Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA. Manual recoding of un-recoded product and substance terms arises from ICSRs. Identification and management of duplicate ICSRs. Activities related to SPOR / IDMP. Quality review of ICSRs. Quality review for the work performed by peers. Serves as a subject matter expert in SPVG, which includes resolution of project related routine queries; mentoring, coaching and training of new hires. Fosters constructive and professional working relationships with all project team members, internal and external. Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities. Ensures distribution of all required individual expedited and periodic reports for both clinical and post-marketing projects to the Safety Submissions team if contracted to submit the reports. Participate in audits/inspections as required. Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate. Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process. Qualifications Bachelor’s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job. Safety Database systems and knowledge of medical terminology required. Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance Proficiency in Microsoft Office Suite (Word, Excel and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace) and internet. Ability to work independently and in a team environment. Excellent communication and interpersonal skills, both written and spoken. Good organizational skills with proven ability to prioritize and work on multiple tasks and projects. Detail oriented with a high degree of accuracy and ability to meet deadlines. Minimal travel may be required (up to 5%). Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Show more Show less

Description Medical Scientist - Shanghai Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner. Attends at Trusted Process meetings and may participate in internal and external audits. Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. Qualifications Degree in life sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific experience and/or training discipline. Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential. A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work. Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership. Understanding of scientific principles to assure effective and high-quality medical data analysis. Excellent written and oral communication skills. Excellent computer skills: MS Office programs, spread sheets, presentations. Prefer knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines. Strong team player with excellent interpersonal skills and ability to work effective in a cross-functional team environment. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Show more Show less

Description Medical Scientist Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner. Attends at Trusted Process meetings and may participate in internal and external audits. Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. Qualifications Degree in life sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific experience and/or training discipline. Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential. A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work. Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership. Understanding of scientific principles to assure effective and high-quality medical data analysis. Excellent written and oral communication skills. Excellent computer skills: MS Office programs, spread sheets, presentations. Prefer knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines. Strong team player with excellent interpersonal skills and ability to work effective in a cross-functional team environment. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Show more Show less

Description Medical Scientist Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. Job Responsibilities Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans. Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews. Authors medical data queries and reviews query responses, approves query closure in association with Medical Director. May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed. Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed. Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review. Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner. Attends at Trusted Process meetings and may participate in internal and external audits. Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology. Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans. Qualifications Degree in life sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific experience and/or training discipline. Excellent time management skills to handle multiple tasks and meet deadlines while delivering high quality work in a highly regulated and dynamic environment is essential. A self-starter and comfortable with fluctuating timelines, work demands and changes in scope of work. Ability to troubleshoot situations as needed and understands when issues or questions need to be escalated to the leadership. Understanding of scientific principles to assure effective and high-quality medical data analysis. Excellent written and oral communication skills. Excellent computer skills: MS Office programs, spread sheets, presentations. Prefer knowledge of drug development and demonstrated proficiency with ICH/GCP guidelines. Strong team player with excellent interpersonal skills and ability to work effective in a cross-functional team environment. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Show more Show less

Alm. Brand Foreningen 1792 søger sin første kommunikationschef med tiltrædelse den 1. august 2025 eller snarest derefter. Har du erfaring fra en børsnoteret virksomhed, interesse i filantropi og formidling af projekter, og er du er en erfaren og strategisk kommunikatør med en bred værktøjskasse og god samfundsforståelse, kan det være dig, vi er på udkig efter. Om os Alm. Brand Foreningen 1792 har ca. 800.000 medlemmer, som er kunderne i de fire forsikringsselskaber i Alm. Brand Group. Foreningen ejer i dag ca. 47 % af aktierne i det børsnoterede Alm. Brand A/S, og foreningens langsigtede interesse er at sikre Alm. Brand A/S som en konkurrencedygtig aktør på det danske forsikringsmarked. Foreningen har inden for de senere år øget sine aktiviteter og opbygget et sekretariat, som blandt andet understøtter foreningens bestyrelse i uddelinger af midler til styrkelse af aktiviteter inden for forsikring og forebyggelse i bred forstand, et stigende antal filantropiske uddelinger og almennyttige aktiviteter inden for området ”Børns og unges trivsel” samt forvaltning af foreningens midler og et aktivt ejerskab af Alm. Brand A/S. Vores nye kommunikationschef vil stå for kommunikationsopgaver inden for alle områderne. Opgaverne Dine Opgaver Vil Primært Bestå i Udvikling og implementering af foreningens kommunikationsstrategi Rollen som redaktør og skribent på vores hjemmeside, SoMe og nyhedsbreve Skrive artikler mv. til årsrapporter og publikationer Sikre indhold til Alm. Brand Groups kanaler om foreningens aktiviteter Pressehåndtering inden for både finansielle og filantropiske medier Sparring om kommunikationsplaner og strategier med støttemodtagere Afvikling af kommunikationsaktiviteter med samarbejdspartnere og støttemodtagere Udvikling og vedligeholdelse af interne produkter, årshjul mv. Bidrage til bestyrelsesmateriale og bestyrelsesbetjening Medvirke til events, møder og administrative driftsopgaver Være sparringspartner for ledelsen om kommunikation Håndterer eksterne leverandører på kommunikationsområdet På sigt opbygning af eget team Om dig Du har både bred og solid erfaring med kommunikationsområdet og meget gerne inden for både børsnoteret virksomhed, filantropi og almennyttige formål. Har du også kendskab til forsikringsbranchen, er det et stort plus. Du kan rumme mange emner og samarbejdsflader og har en positiv tilgang til dine opgaver og kollegaer. Som person er du struktureret og fokuseret og har både øje for detaljer i dit arbejde og sammenhængen til dine kollegaers opgaver. Du lægger vægt på at være en positiv og løsningsorienteret kollega og har arbejdserfaringer med at opbygge gode relationer til meget forskellige interne og eksterne samarbejdspartnere. Det er afgørende, at du har lyst til at medvirke konstruktivt og åbent i opbygning af foreningens sekretariat, hvor vi både har faste opgaver men også samarbejder på kryds og tværs. Du skal være initiativrig og lyttende og kunne prioritere dine konkrete arbejdsopgaver og bevare overblikket – og ikke mindst det gode humør. Vi Er På Udkig Efter Ansøgere, Som er uddannet inden for journalistik, kommunikation, retorik, samfundsfag mv. har mindst 5 års relevant erhvervserfaring som fuldtidsansat kan udvikle og eksekvere strategisk inden for flere felter har en bred værktøjskasse og kan producere til mange platforme kan finde gode vinkler i både foreningens finansielle og filantropiske arbejde har erfaringer med erhvervsmedier og presserådgivning vil styre efter planer, men også griber spontane muligheder har erfaringer med eller stor interesse for foreningens uddelingsområder kan sikre en stærk og bred kommunikation, der understøtter foreningens formål og aktiviteter. Vi tilbyder Vi tilbyder et udfordrende og spændende job i en lille organisation under opbygning og med store ambitioner om at gøre en forskel på alle vores aktivitetsområder. Hos os vil du få en meget afvekslende vifte af opgaver inden for både den finansielle sektor og et løbende samspil med Alm. Brand Groups presse- og kommunikationsafdelinger og samtidig et tæt samarbejde med foreningens engagerede uddelingsteam, som ledes af vores uddelingschef, samt med resten af sekretariatet. Du vil få gode muligheder for selv at opbygge kommunikationsområdet og vil have mulighed for at anvende eksterne leverandører eller en medarbejder, hvis behov er til stede. Du vil referere direkte til direktør Tue Klitgaard Christensen og have et tæt samarbejde med uddelingschef Laura Auken Larsen. Ansøgning og kontakt Har du spørgsmål til jobbet, er du velkommen til at kontakte direktør Tue Klitgaard Christensen på tlf. 51 29 27 35 eller e-mail abtuci@almbrand.dk. Send venligst en motiveret ansøgning og CV samt gerne også konkrete produkter eller links dertil ved at klikke på ”Ansøg om dette job” senest mandag 2. juni 2025. Vi gør opmærksom på, at vi behandler ansøgningerne løbende, og vi lukker for yderligere ansøgninger, når vi har fundet den rigtige kandidat. For en god ordens skyld gør vi også opmærksom på, at vores nuværende hjemmeside er under udvikling og ikke indeholder materiale til ansøgere eller vores uddelinger. Disse kan du se på vores LinkedIn-profil: https://dk.linkedin.com/company/alm-brand-foreningen-1792 Vi glæder os til at høre fra dig! Show more Show less

Pavago is an offshore recruitment company specializing in building remote teams by connecting companies with top talent from regions including Latin America, Pakistan, the Philippines, and South Africa. Our client, represented by Pavago, is a values-driven education and coaching company that empowers business owners to build more profitable, systemized companies. By offering tools, training, and a strong community, the client helps contractors increase profit, streamline operations, and reclaim their time through better systems and stronger leadership. Applications at getonbrd.com. Key Responsibilities Organic Growth & Facebook Group Management: Proven experience in growing and managing Facebook groups organically, demonstrating a successful track record in this area. Expertise in Facebook growth hacks, organic content strategies, and managing multiple accounts (20+). Copywriting: You will be the go-to expert in copywriting, with deep, hands-on experience. You understand exactly what makes a copy effective and impactful. Content and Creation Strategy: Develop and implement strategic initiatives to grow and optimize our Facebook groups. This includes increasing leads, improving engagement, and expanding into new industries. Social Media Development: Establish and grow social media accounts from the ground up, turning them into vibrant, top-performing channels with a strong following. Leading and Overseeing Copy and Content Writing Efforts: Devote the majority of their time to crafting and approving content for clients' Facebook Groups and social media accounts, ensuring it aligns with the client’s vision and mission. Client Success & Communication: Lead client-facing efforts, ensuring exceptional client satisfaction. Regularly meet with clients to review progress, discuss future strategies, and align on the vision. KPI Management: Take charge of the team’s KPIs, ensuring that goals are met consistently. Monitor and report on performance metrics, making data-driven decisions to improve results. Team Leadership: Experienced in effectively leading and motivating teams to achieve success. Role Description And Required Experience We are seeking a dynamic and experienced Marketing Director with a strong background in organic marketing and community management on Facebook Groups. The ideal candidate will have a proven ability to grow and engage multiple Facebook Communities organically while creating compelling content that resonates with diverse audiences. This role demands exceptional copywriting skills and a deep understanding of organic growth strategies specific to Facebook Groups. Candidates must have experience managing large teams and driving business growth through social media channels. Key Qualifications Include Facebook Group Organic Marketing: Possesses experience in elevating local businesses through Organic Marketing in Facebook Groups, with a creative flair for developing compelling content and managing engaging social media accounts. Copy and Content Writer: The ideal candidate is an exceptional writer whose skills have significantly elevated social media accounts. They excel at capturing the attention of potential readers and driving engagement through impactful writing. Team Leadership & Motivation: Lead a team of 10+ members, prioritizing motivation, productivity, and maintaining high energy levels. Develop incentive structures to enhance performance and retain top talent. Relationship Building: Foster strong, lasting relationships with clients to ensure their needs are met and exceeded. Scaling & Growth: Identify and capitalize on opportunities to scale the business, exploring new marketing channels, sales strategies, and industry verticals. Drive the growth of the Facebook Groups business from $500k ARR to over $1M. Innovation & Improvement: Constantly seek opportunities to enhance our services, attract the right clients, and stay ahead of industry trends. Preferred But Not Required Skills Additional strengths that will distinguish candidates include: Experience in other social media platforms beyond Facebook, such as Instagram, LinkedIn, or TikTok, with an organic growth focus. Background in content marketing strategy with the ability to integrate cross-channel campaigns. Knowledge of analytics tools to further optimize campaign efforts and audience segmentation. Prior work experience with clients in construction, accounting, or financial services industries. A passion for continuous learning and staying abreast of evolving social media trends and Facebook algorithm changes. What We Offer We provide a structured and reliable remote work environment supported by essential technology and connectivity tools to empower productivity and ensure seamless communication. The hiring process is thorough, including phone screening, video interviews, practical creative assessments, and final client meetings to ensure an excellent cultural and professional fit. This role offers the unique opportunity to contribute to a high-profile client handling construction and software projects, with a dedicated and high-achieving marketing team. The position works EST hours, catering exclusively to candidates living in Mexico to foster a regionally aligned remote culture. GETONBRD Job ID: 53925 Remote work policy Locally remote only Position is 100% remote, but candidates must reside in Peru, Chile, Colombia, Costa Rica, Guatemala, Argentina, Mexico, Honduras, Nicaragua, Bolivia, Jamaica, Paraguay or Brazil. Show more Show less

Leniolabs_ es ahora Improving South America! Somos una empresa internacional de desarrollo de software con miembros de equipos en Argentina, Chile, España y USA principalmente. Colaboramos en el desarrollo de software de nuestros clientes, sumándonos con nuestros equipos y estructura, trabajando directamente con los clientes los cuales se encuentran mayoritariamente en San Francisco. Trabajamos con equipos distribuidos, de manera remota y colaborativa, utilizando herramientas como Slack, Zoom, HO, Jira, etc. Nuestra experiencia se basa fuertemente en frontend development y También trabajamos en desarrollo backend. Valoramos a las personas dinámicas en el aprendizaje de nuevas tecnologías para utilizarlas en los proyectos. Opportunity published on Get on Board. Funciones del cargo En Improving South America buscamos un/a ✶ Senior Node.js Cloud Developer ✶ para sumarse a un proyecto global enfocado en el desarrollo de un producto de gestión financiera, en colaboración directa con un cliente con presencia en Canadá, EE.UU., Europa y Asia. Estamos en busca de un perfil senior con sólida experiencia en Node.js y TypeScript, capaz de diseñar soluciones escalables en entornos Serverless sobre AWS. Responsabilidades Principales Desarrollo backend con Node.js + TypeScript, asegurando calidad, performance y escalabilidad. Implementación de arquitecturas Serverless y Event-Driven. Gestión de funciones y servicios sin servidor con Serverless Framework. Integración de servicios AWS como Lambda, API Gateway, EventBridge, SNS, SQS y Step Functions. Infraestructura como código utilizando Terraform o AWS CDK. Trabajo en equipo junto a perfiles internacionales, participando en decisiones técnicas clave. Skill requerido +10 años de experiencia en desarrollo de software. +5 años desarrollando con Node.js (indispensable). Experiencia sólida en TypeScript (indispensable). Dominio en desarrollo Serverless y arquitectura Event-Driven. Experiencia con servicios AWS: Lambda, API Gateway, EventBridge, SNS, SQS, Step Functions. Conocimiento y experiencia con IaC: Terraform o AWS CDK. Experiencia comprobable en entornos AWS (prioritario sobre otras nubes). Nivel de inglés intermedio/avanzado (excluyente). Certificación en AWS (bonus). Fuertes habilidades de comunicación, trabajo en equipo, organización y gestión del tiempo. Beneficios Salario dolarizado (Argentina) Metlife (Chile) 100% Remoto. Posibilidad de recibir 2 bonos al año 2 revisiones salariales al año Vacaciones Clases de inglés Equipamiento Apple Cursos UDEMY Budget para compra de libros Budget para compra de materiales de trabajo GETONBRD Job ID: 53789 Flexible hours Flexible schedule and freedom for attending family needs or personal errands. Internal talks Improving South America offers space for internal talks or presentations during working hours. Computer provided Improving South America provides a computer for your work. Remote work policy Locally remote only Position is 100% remote, but candidates must reside in Argentina, Colombia, Chile, Peru or Uruguay. Show more Show less

Pavago is an offshore recruitment company specializing in building remote teams by connecting companies with top talent from regions including Latin America, Pakistan, the Philippines, and South Africa. Our client, represented by Pavago, is a values-driven education and coaching company that empowers business owners to build more profitable, systemized companies. By offering tools, training, and a strong community, the client helps contractors increase profit, streamline operations, and reclaim their time through better systems and stronger leadership. Find this vacancy on Get on Board. Key Responsibilities Organic Growth & Facebook Group Management: Proven experience in growing and managing Facebook groups organically, demonstrating a successful track record in this area. Expertise in Facebook growth hacks, organic content strategies, and managing multiple accounts (20+). Copywriting: You will be the go-to expert in copywriting, with deep, hands-on experience. You understand exactly what makes a copy effective and impactful. Content and Creation Strategy: Develop and implement strategic initiatives to grow and optimize our Facebook groups. This includes increasing leads, improving engagement, and expanding into new industries. Social Media Development: Establish and grow social media accounts from the ground up, turning them into vibrant, top-performing channels with a strong following. Leading and Overseeing Copy and Content Writing Efforts: Devote the majority of their time to crafting and approving content for clients' Facebook Groups and social media accounts, ensuring it aligns with the client’s vision and mission. Client Success & Communication: Lead client-facing efforts, ensuring exceptional client satisfaction. Regularly meet with clients to review progress, discuss future strategies, and align on the vision. KPI Management: Take charge of the team’s KPIs, ensuring that goals are met consistently. Monitor and report on performance metrics, making data-driven decisions to improve results. Team Leadership: Experienced in effectively leading and motivating teams to achieve success. Role Description And Required Experience We are seeking a dynamic and experienced Marketing Director with a strong background in organic marketing and community management on Facebook Groups. The ideal candidate will have a proven ability to grow and engage multiple Facebook Communities organically while creating compelling content that resonates with diverse audiences. This role demands exceptional copywriting skills and a deep understanding of organic growth strategies specific to Facebook Groups. Candidates must have experience managing large teams and driving business growth through social media channels. Key Qualifications Include Facebook Group Organic Marketing: Possesses experience in elevating local businesses through Organic Marketing in Facebook Groups, with a creative flair for developing compelling content and managing engaging social media accounts. Copy and Content Writer: The ideal candidate is an exceptional writer whose skills have significantly elevated social media accounts. They excel at capturing the attention of potential readers and driving engagement through impactful writing. Team Leadership & Motivation: Lead a team of 10+ members, prioritizing motivation, productivity, and maintaining high energy levels. Develop incentive structures to enhance performance and retain top talent. Relationship Building: Foster strong, lasting relationships with clients to ensure their needs are met and exceeded. Scaling & Growth: Identify and capitalize on opportunities to scale the business, exploring new marketing channels, sales strategies, and industry verticals. Drive the growth of the Facebook Groups business from $500k ARR to over $1M. Innovation & Improvement: Constantly seek opportunities to enhance our services, attract the right clients, and stay ahead of industry trends. Preferred But Not Required Skills Additional strengths that will distinguish candidates include: Experience in other social media platforms beyond Facebook, such as Instagram, LinkedIn, or TikTok, with an organic growth focus. Background in content marketing strategy with the ability to integrate cross-channel campaigns. Knowledge of analytics tools to further optimize campaign efforts and audience segmentation. Prior work experience with clients in construction, accounting, or financial services industries. A passion for continuous learning and staying abreast of evolving social media trends and Facebook algorithm changes. What We Offer We provide a structured and reliable remote work environment supported by essential technology and connectivity tools to empower productivity and ensure seamless communication. The hiring process is thorough, including phone screening, video interviews, practical creative assessments, and final client meetings to ensure an excellent cultural and professional fit. This role offers the unique opportunity to contribute to a high-profile client handling construction and software projects, with a dedicated and high-achieving marketing team. The position works EST hours, catering exclusively to candidates living in Mexico to foster a regionally aligned remote culture. GETONBRD Job ID: 53925 Remote work policy Locally remote only Position is 100% remote, but candidates must reside in Peru, Chile, Colombia, Costa Rica, Guatemala, Argentina, Mexico, Honduras, Nicaragua, Bolivia, Jamaica, Paraguay or Brazil. Show more Show less

Job title: Patent Attorney (PQ or FQ), Digital (Physics) Discipline: Engineering/Maths/Physics with strong computing component Technologies: Ability to work in complex mathematical fields such as artificial intelligence, machine learning models, mathematical modelling, fluid dynamics, thermodynamics, acoustics, statistical analysis, cryptography, quantum computing, post-quantum techniques. Preferred minimum level of qualification: 1st Class Degree - Batchelors/Masters/Doctorate EIP tech group: Digital Seniority: Part-qualified/Qualified Term: Permanent Working hours: Full-time (3 days in the office & 2 from home) About EIP Digital EIP Digital encompasses a broad technology spectrum including computer hardware, software and machine learning/AI, electronics, wireless and telecommunications, applied physics and optics. Strength in these fields has been at the core of EIP and our continued success since we were founded in 2000. Renowned for its experience in patent drafting and strategic patent prosecution, and a go-to practice for litigation in high-tech patent cases, EIP's Digital team has been engaged in many of the highest profile patent litigation cases in the UK and Germany, and oppositions at the EPO, in recent years. EIP Digital team members are appointed to many high-value matters which require extraordinary levels of expertise, including licensing, technology standards, pre-litigation analysis, and litigation itself, with high rates of success. Many of these members operate at the intersection of various cutting areas such as electronics and health-tech, AI and drug discovery. About The Vacancy We are looking for patent attorneys from all levels who are capable of handling maths-heavy technologies, such as artificial intelligence (AI), machine learning, cryptography, and similar high-tech digital technologies. Successful candidates will have a background in mathematics, physics, computer science or engineering. Although qualification to PhD level is preferred, we will consider any candidate with a strong first or further degree who demonstrates the required skill and knowledge to handle these technologies. Experience, Skills & Qualifications You will be comfortable working in a modern, fast-paced environment where you are given a level of autonomy to do your work. Successful candidates will also be able to demonstrate the following: Excellent academics An appropriate professional attitude (personable, well prepared, flexible and enthusiastic) Excellent written and oral communication skills Ability to express complex ideas clearly and concisely, and the ability to structure a precise and coherent argument Ability to deal with a variety of people at different levels Ability to balance knowledge of intellectual property law against commercial requirements Ability to work under pressure, which may be the result of competing and inflexible deadlines when working for more than one client at the same time Excellent research and presentation skills Meticulous attention to detail, and an analytical mind Initiative and the ability to act independently and manage own workload About EIP EIP is award-winning patent firm which and specialises in high-value and complex patent matters. In 2024 EIP won Managing IP’s ‘European Patent Contentious Firm of the Year’ award and for the sixth year in a row. EIP has been ranked in the FT's list of Europe’s Leading Patent Law Firms and is one of only three firms in Europe to achieve a gold ranking in each of their six categories. EIP has around 185 employees who operate from six European offices (London, Bath, Leeds, Cardiff, Stockholm and Düsseldorf) as well as one office in the US (Denver). Our multidisciplinary team combines patent attorneys, litigators and commercial IP lawyers, has an impressive global client base from SMEs to multinational blue-chip companies and includes telecoms owners, major software developers, pharma and biotech companies, medical device manufacturers, aerospace and logistics companies. Diversity is an intrinsic part of EIP’s business culture. We are proud to support the IP Inclusive initiative, and we are a signatory to the IP Inclusive Charter. EIP actively engages in diversity efforts and is committed to developing an attitude of openness for the benefit of all those working in the IP profession. Other Information With our state-of-the-art tech platform, we offer hybrid working, three days in the office and two from home. EIP’s employees also enjoy reduced business hours on the days when working from the office subject to there being no urgent work commitments. EIP has a friendly, progressive and mutually supportive working environment along with a smart casual dress policy and stylish modern offices. Show more Show less

33369BR Bangalore - Campus Job Description Job Title: Assistant Vice President—Telecom Delivery Leader Experience: 20+ Years Industry: Telecom | Product Engineering | Services Role Overview We are seeking a seasoned Delivery Leader with extensive experience managing large-scale, complex telecom projects and customer relationships, including Tier-1 Telco clients. This leadership role requires a strong understanding of telecom platforms and products, coupled with strategic delivery oversight. The ideal candidate will lead a large team, cross-functional global delivery team comprising architects, leads, engineers, and testers. Key Responsibilities Drive successful end-to-end delivery of multi-tower telecom projects (deployment, development, testing). Manage P&L, delivery KPIs, quality, cost, and schedule across all engagement streams. Build and maintain strong customer relationships at leadership levels; act as the primary escalation point. Lead teams working on products and streams such as UIV, FlowOne, NORc, NAC, Assurance, Security, Analytics. Drive end to end delivery and Enable delivery excellence across platform engineering, adapter development, and inventory systems. Provide strategic direction, resource planning, and risk mitigation for high-performance delivery. Collaborate with technical leads across skill towers: Kubernetes, OCP, NCS, AWS, Java, Shell Scripting, Spring Boot, BPMN, REST/SOAP, CI/CD tools, and test automation frameworks. Required Skills & Expertise Proven telecom domain experience with large product/platform-based engagements. Delivery leadership across products like FO, UIV, NORc, NAC and platform tools (Kubernetes, Docker, Linux). Strong technical acumen across system architecture, automation, and test engineering. Exposure to telecom ecosystems and telecom inventory systems is a strong advantage. Proficiency in managing geographically distributed teams and complex stakeholder landscapes. Preferred Qualifications B.E./B.Tech/MCA or equivalent technical degree. Telecom certifications (preferred). Experience working with agile and DevOps methodologie Qualifications MCA, MTECH, BE Range of Year Experience-Min Year 20 Range of Year Experience-Max Year 20 Show more Show less

33366BR Georgia Job Description Product Owner Qualifications Graduate Range of Year Experience-Min Year 8 Range of Year Experience-Max Year 10 Show more Show less

32370BR Chennai Job Description Technical Project Manager Manage project technical team on daily basics, including specific tasks assignment and control of their execution, coordinate engineer’s work according to customer demands and expectation. Schedule and facilitate regular Project technical meetings. Provides report about the status, existing issues, future plans according to responsibility area Accountable for quality of all technical process and procedures implemented at the project, e.g. customer network intervention: administrative and technical preparations of such Interventions, including development of all required procedures and their rehearsal testing in labs, instructing intervention engineers, making decision about the results of Intervention execution. For failed Intervention or/and for customer network outages, caused by the Intervention, responsible to provide RCA, list of corrective and preventive actions, secure the actions implementation. Accountable and responsible for closure and follow up of all Tickets raised towards Salesforce/4LS/R&D. Accountable for tickets consolidation, prioritization and escalation. Responsible for Kick of call of upgrade project and discuss the requirements during upgrade e.g. MW length, Traffic migration, SOW, Deliverables, exclusions etc. Defines SW upgrade strategy, including recommendation & decision of target SW version for Network Elements (NE), their upgrade sequence, considering dependency from other NEs of the Nokia solution. Accountable for Project technical documents study, release notes study compatibility matrix compliance, according to customer and internal procedures Accountable for creation of upgrade assessment document for customer which explains what all SW bugs/problems fixed in SW version and new features etc. Responsible for Assignments of Network Element for upgrade Responsible for Maintenance window coordination with various customer and internal SPOCs during upgrade execution HOW YOU WILL CONTRIBUTE AND WHAT YOU WILL LEARN Responsible for domain project delivery schedule creation. Responsible to support Project Manager in creation of Project schedule and Resource Management plan Responsible for definition of the required resources, alignment of the resource demand with DDM, TDL Accountable for Project technical documents initiation, creation, and delivery, according to customer and internal procedures Accountable for design documents delivery according to customer and project requirements Accountable for technical project scope delivery, including network functions deployment, integration, upgrade, acceptance testing, system performance evaluation. Accountable to consult Project stakeholders with all technical questions related to CPC Defines SW implementation strategy, including specific SW version for Network Elements (NE), their installation sequence, considering dependency from other NEs of the Nokia solution. Defines the requirement for new SW features development, required for project completion. Interworks with R&D and Product Managers to request those features. Responsible for managing of project technical risks Defines and implement new tools to increase project execution effectiveness, including automation tools, provides feedback toward tools developers. KEY SKILLS AND EXPERIENCE Around 15+ years of experience in Packet Core Projects Knowledge and Experience for Packet Core Equipment: MME, S/PGW, AMF, SMF, UPF Knowledge and Experience for Nokia Packet Core equipment: cMM, cMG, NRD Capable of understanding Technical Notes, Protocol Specs, Method of Procedure Linux knowledge is an advantage Basic understanding of Project Management skill is an advantage Computer: MS Office, Teams Qualifications B.Tech Range of Year Experience-Min Year 12 Range of Year Experience-Max Year 15 Show more Show less

33152BR Bangalore Job Description 7+ yrs of relevant experience and have worked in at lease 2-3 Workday BIRT (Business Intelligence and Reporting Tools) projects as a Senior Developer Workday BIRT (Business Intelligence and Reporting Tools) Have strong understanding of key modules of Workday and necessary workflows within Workday Strong client communication and ability to work with US stakeholders independently without assistance Ready to work during overlapping hours during US EST morning. Qualifications BE Range of Year Experience-Min Year 7 Range of Year Experience-Max Year 9 Show more Show less

33388BR Georgia Job Description Senior Program Manager Qualifications Graduate Range of Year Experience-Min Year 8 Range of Year Experience-Max Year 10 Show more Show less

Wil jij deel uitmaken van het MoVE team dat processen, ruimtes en labo’s binnen de farmaceutische sector analyseert, test en valideert? Senior Mobile Validation Engineer Functieomschrijving Je bent verantwoordelijk voor het kwalificeren en valideren van GMP-kritische sytemen zoals cleanrooms, temperatuur gecontroleerde ruimtes, labosystemen , HVAC en nutsvoorzieningen bij onze klanten. Je denkt met de klant mee na over oplossingen om de GMP-kritische systemen compliant te krijgen aan de geldende wetgevingen en vereisten. Ook ben je betrokken bij het opstellen van protocollen, rapporten en verbetervoorstellen, en geef je opleidingen aan collega’s en klanten. De internationale wetgeving, richtlijnen en evoluties binnen de sector volg je op de voet en je houdt kennis up-to-date. Je fungeert als de belangrijkste contactpersoon voor klanten en leveranciers, waarbij je zorgt voor een soepele communicatie en samenwerking. Bovendien ben je betrokken bij het hele business proces van het opstellen van offertes tot facturatie. Je volgt het kwaliteitssysteem op en biedt ondersteuning in de uitvoering van interne audits en optimalisaties van processen Profiel Je hebt uitgebreide ervaring met cleanroomvalidatietesten, sterilisatievalidatie, mappingen en kalibraties of in één van deze domeinen. Zorgvuldigheid is je tweede natuur. Je streeft telkens naar perfectie. Overleggen, overtuigen, informeren, bijsturen… vlot communiceren is jouw ding. Je houdt van afwisseling tussen het hands-on werken en je administratie. Je bent flexibel en kan je makkelijk aanpassen aan de wensen van de klant. Je spreekt Nederlands en Engels, andere talen zijn mooi meegenomen. Aanbod Je komt terecht in een dynamisch bedrijf in volle groei met een no-nonsens cultuur waar we eigen initiatief toejuichen. Je maakt deel uit van een hecht team, “The A-team”. Door diverse teamactiviteiten leer je jouw collega’s beter kennen: sportactiviteiten, een quiz, verrassingsdiner, after work drink in de zomerbar, … Je komt op veel plaatsen, we voorzien een vergoeding en verblijf voor je reizen naar het buitenland. We werken samen, houden elkaar scherp en inspireren elkaar: denktanks, focusgroepen, brainstorms, … Uitdaging, opleidingen, doorgroeimogelijkheden én de kans je job zelf mee vorm te geven. Show more Show less

Ben jij een ervaren professional in de life sciences en werk je als freelancer? Sluit je aan bij Advipro en zet jouw expertise in voor boeiende projecten die er écht toe doen! Wat kun je verwachten als freelance consultant bij Advipro? Bij Advipro Waarderen We Jouw Ervaring En Zetten We Die In Om Sleutelprojecten Binnen De Life Sciences Te Leiden, Ondersteunen En Coördineren Je werkt samen met toonaangevende bedrijven in de farmaceutische industrie, biotech, cosmetica, gezondheidszorg . Ontdek hier meer over de sectoren waarin Advipro actief is. Afhankelijk van jouw kennis en ambities werk je aan grote, uitdagende projecten op afdelingen zoals QA, Engineering, Validatie, Operaties of Productie. Je blijft up-to-date met internationale wetgeving, richtlijnen en trends binnen de sector. Je pakt uitdagingen aan met een oplossingsgerichte en pragmatische houding. Wie zoeken we? Je hebt aantoonbare ervaring in de farmaceutische industrie, biotech, medische hulpmiddelen, cosmetica of gezondheidszorg. Je bent goed thuis in GxP-regels, ISO-normen en industriestandaarden (zoals FDA, Eudralex, MDR, MHRA, FAGG, ICH, ISPE, PIC/S, enz.). Je hebt expertise in één of meer van de volgende vakgebieden: Validatie, Kwalificatie & Commissioning Engineering Kwaliteitsborging Kwaliteitscontrole Product Support / CMC Je bent communicatief sterk en spreekt vloeiend Nederlands en Engels (extra talen zijn mooi meegenomen). Waarom Advipro? We creëren maatwerkafspraken die aansluiten bij jouw behoeften en de geldende wet- en regelgeving voor freelancers. Bij Advipro bouw je aan langdurige, waardevolle relaties en word je onderdeel van ons A-Team. We stimuleren jouw ontwikkeling met leer- en groeimogelijkheden. Als een ambitieus en dynamisch bedrijf bieden we de ideale omgeving om te schitteren in de life sciences. Klaar voor de volgende stap? Stuur ons je CV en wie weet verwelkomen we jou binnenkort in ons A-team! Show more Show less

Leniolabs_ es ahora Improving South America! Somos una empresa internacional de desarrollo de software con miembros de equipos en Argentina, Chile, España y USA principalmente. Colaboramos en el desarrollo de software de nuestros clientes, sumándonos con nuestros equipos y estructura, trabajando directamente con los clientes los cuales se encuentran mayoritariamente en San Francisco. Trabajamos con equipos distribuidos, de manera remota y colaborativa, utilizando herramientas como Slack, Zoom, HO, Jira, etc. Nuestra experiencia se basa fuertemente en frontend development y También trabajamos en desarrollo backend. Valoramos a las personas dinámicas en el aprendizaje de nuevas tecnologías para utilizarlas en los proyectos. Send CV through Get on Board. Funciones del cargo En Improving South America buscamos un/a ✶ Senior Node.js Cloud Developer ✶ para sumarse a un proyecto global enfocado en el desarrollo de un producto de gestión financiera, en colaboración directa con un cliente con presencia en Canadá, EE.UU., Europa y Asia. Estamos en busca de un perfil senior con sólida experiencia en Node.js y TypeScript, capaz de diseñar soluciones escalables en entornos Serverless sobre AWS. Responsabilidades Principales Desarrollo backend con Node.js + TypeScript, asegurando calidad, performance y escalabilidad. Implementación de arquitecturas Serverless y Event-Driven. Gestión de funciones y servicios sin servidor con Serverless Framework. Integración de servicios AWS como Lambda, API Gateway, EventBridge, SNS, SQS y Step Functions. Infraestructura como código utilizando Terraform o AWS CDK. Trabajo en equipo junto a perfiles internacionales, participando en decisiones técnicas clave. Skill requerido +10 años de experiencia en desarrollo de software. +5 años desarrollando con Node.js (indispensable). Experiencia sólida en TypeScript (indispensable). Dominio en desarrollo Serverless y arquitectura Event-Driven. Experiencia con servicios AWS: Lambda, API Gateway, EventBridge, SNS, SQS, Step Functions. Conocimiento y experiencia con IaC: Terraform o AWS CDK. Experiencia comprobable en entornos AWS (prioritario sobre otras nubes). Nivel de inglés intermedio/avanzado (excluyente). Certificación en AWS (bonus). Fuertes habilidades de comunicación, trabajo en equipo, organización y gestión del tiempo. Beneficios Salario dolarizado (Argentina) Metlife (Chile) 100% Remoto. Posibilidad de recibir 2 bonos al año 2 revisiones salariales al año Vacaciones Clases de inglés Equipamiento Apple Cursos UDEMY Budget para compra de libros Budget para compra de materiales de trabajo GETONBRD Job ID: 53789 Flexible hours Flexible schedule and freedom for attending family needs or personal errands. Internal talks Improving South America offers space for internal talks or presentations during working hours. Computer provided Improving South America provides a computer for your work. Remote work policy Locally remote only Position is 100% remote, but candidates must reside in Argentina, Colombia, Chile, Peru or Uruguay. Show more Show less

Somos una corporación multinacional de bebidas y alimentos fundada en 1885 con operaciones en más 14 países, con más de 15,000 colaboradores. Tenemos el portafolio de bebidas más grande de la región, y contamos con socios estratégicos como PepsiCo y AB InBev. El último año hemos tenido una expansión a nivel global que nos ha llevado a dividirnos en 4 unidades de negocio: apex (transformación), cbc (distribución), beliv (innovación en bebidas) y bia (alimentos); y como parte de nuestra estrategia dinámica de expansión y crecimiento requerimos talentos para unirse a nuestra corporación. Apply directly at getonbrd.com. Funciones del cargo Diseñar e implementar soluciones de ingeniería de datos escalables, eficientes y mantenibles utilizando tecnologías como Azure Data Factory (ADF), Databricks y Unity Catalog, aplicando arquitecturas por capas (Bronze/Silver/Gold), automatización de ETL/ELT con validación de calidad de datos, y estrategias de integridad como pipelines idempotentes y manejo de SCD. El objetivo es garantizar datos confiables, optimizados en costos y performance, alineados con las necesidades del negocio, respaldados por documentación robusta y estándares de código (PEP8, Git) para facilitar su evolución y gobierno. Requerimientos del cargo Coordinar el funcionamiento de los distintos entornos donde se ejecutan los procesos de procesamiento de datos. Extraer, transformar y cargar los datos para que estén alineados con respecto a las necesidades del negocio. Generar integraciones eficientes que permitan realizar la ingesta de datos requeridos para la lógica de negocio. Generar flujos de integración continua que permitan validar los flujos desarrollados de forma eficaz. Mentorizar a igenieros juniors en buenas practicas y soluciones escalables. Proponer e implementar mejoras tecnologicas que optimicen los flujos de datos. Principales Retos Requiere criterio para diseñar, implementar y mantener una estructura de datos eficiente, escalable e intuitiva. Requiere criterio y experiencia para cumplir con las mejores prácticas de código para el desarrollo de funcionalidades competitivas en el mercado. Procesar volúmenes de datos en crecimiento exponencial sin que los costos en la nube se disparen. Implementar mecanismos de data quality que no impacten la velocidad de los procesamientos. GETONBRD Job ID: 53848 Conditions Health coverage Global Mobility Apex, S.A. pays or copays health insurance for employees. Computer provided Global Mobility Apex, S.A. provides a computer for your work. Informal dress code No dress code is enforced. Remote work policy Locally remote only Position is 100% remote, but candidates must reside in Chile, Colombia, Ecuador, Peru, Mexico, Guatemala or El Salvador. Show more Show less

En Alegra contamos con un equipo de más de 500 personas trabajando 100% remoto con una cultura única, innovadora y dinámica, que está revolucionando cómo las Pymes gestionan sus finanzas con un ecosistema de soluciones digitales en la nube disponible en 8 países en Latam, España y ¡vamos por más! 🚀 This company only accepts applications on Get on Board. Tu misión en Alegra Serás responsable del producto asignado, con el objetivo de crear soluciones fáciles y prácticas para emprendimientos, pymes , profesionalescontables y administradores . Tendrás la misión de transmitir la visión del producto al equipo y a la compañía, colaborar de cerca con diseño, priorizarfuncionalidades y liderar el roadmap , alineando a los distintos stakeholders para asegurar entregas a tiempo y con alto impacto . Planear, diseñar y construir nuevas soluciones en los productos de Alegra, liderando las tareas del área de diseño y desarrollo. Comunicar frecuentemente y de manera interna y clara, las nuevas funcionalidades y mejoras importantes que ya se encuentran en producción. Conocer todo el customer journey, para pedir y documentar mejoras. Vincularse con todos los equipos de Alegra y liderar nuevos lanzamientos, mejoras y/o cambios importantes. Priorizar sus funciones para documentar nuevas funcionalidades y mejoras de acuerdo a los Objetivos y Resultados clave de Alegra. Probar la función para validar que la UX sea la mejor posible, reportando hallazgos al equipo de ingeniería por la creación y definicióndeissues. Apoyar en todas las etapas del producto, identificando problemas a solucionar por medio de pruebas de usabilidad internas, gestionando las sesiones de experiencia de usuarios reales, y apoyando en la mejora continua de la herramienta y relación con diferentes stakeholders de Alegra. Documentar y crear tareas para los diferentes sub-equipos de producto, y el equipo de diseño, a fin de implementar mejoras y/o cambios con base en lo detectado en la interacción con los usuarios, y/o normativa. Liderar pruebas de usabilidad, documentar mejoras y priorizarlas con base en roadmap de producto. ¿Qué esperamos de ti? Buscamos profesionales con formación en Ingeniería Industrial o áreas afines que posean experiencia en manejo y control de inventarios , capaces de asumir un rol de liderazgo orientado al usuario y con fuerte capacidad de análisis. Debes ser una persona curiosa, adaptable y proactiva que se sienta cómoda exploran Habilidades técnicas Reconocer patrones de navegación en la aplicación. Nivel de inglés B2, C1, o superior. Es un plus si… Contar con experiencia en análisis y manejo de herramientas de datos como Google Analytics, Amplitude, Amazon QuickSight o Google Sheets, que faciliten la interpretación de tableros de métricas y la toma de decisiones basadas en datos. Capacidad para idear, proponer y desarrollar nuevas funcionalidades e innovaciones para el producto que agreguen valor significativo a los usuarios. Tener visión amplia acerca de productos SaaS, especialmente los relacionados con contabilidad, administración, nómina, liquidación y facturación, lo que permitirá comprender y anticipar las necesidades del mercado y usuarios. Alégrate con… ⭐️ Desempeñar tu rol haciendo lo que amas en un entorno 100% remoto, que promueve la autonomía y flexibilidad esperando de ti un alto compromiso. Contar con una relación laboral estable y a largo plazo como empleado full time. Compartir con un equipo multicultural y diverso que trasciende fronteras y culturas, fomentando un ambiente inclusivo e innovador. Contar con recursos para potenciar tu aprendizaje con acceso a plataformas educativas, certificaciones, capacitaciones constantes y una biblioteca virtual. Dos días adicionales de cuidado al año, y programas de bienestar incluyendo mindfulness, alimentación saludable y actividades físicas. Recibir un apoyo económico para optimizar y equipar tu espacio de trabajo remoto. Disfrutar beneficios especiales como bono y medio día libre en tu cumpleaños, además de clases de inglés y coaching para potenciar tu crecimiento personal y profesional. GETONBRD Job ID: 53846 Remote work policy Locally remote only Position is 100% remote, but candidates must reside in Colombia, Argentina, Costa Rica, Mexico or Dominican Republic. Show more Show less

Job title: Patent Attorney (PQ or FQ), Digital (Physics) Discipline: Engineering/Maths/Physics with strong computing component Technologies: Ability to work in complex mathematical fields such as artificial intelligence, machine learning models, mathematical modelling, fluid dynamics, thermodynamics, acoustics, statistical analysis, cryptography, quantum computing, post-quantum techniques. Preferred minimum level of qualification: 1st Class Degree - Batchelors/Masters/Doctorate EIP tech group: Digital Seniority: Part-qualified/Qualified Term: Permanent Working hours: Full-time (3 days in the office & 2 from home) About EIP Digital EIP Digital encompasses a broad technology spectrum including computer hardware, software and machine learning/AI, electronics, wireless and telecommunications, applied physics and optics. Strength in these fields has been at the core of EIP and our continued success since we were founded in 2000. Renowned for its experience in patent drafting and strategic patent prosecution, and a go-to practice for litigation in high-tech patent cases, EIP's Digital team has been engaged in many of the highest profile patent litigation cases in the UK and Germany, and oppositions at the EPO, in recent years. EIP Digital team members are appointed to many high-value matters which require extraordinary levels of expertise, including licensing, technology standards, pre-litigation analysis, and litigation itself, with high rates of success. Many of these members operate at the intersection of various cutting areas such as electronics and health-tech, AI and drug discovery. About The Vacancy We are looking for patent attorneys from all levels who are capable of handling maths-heavy technologies, such as artificial intelligence (AI), machine learning, cryptography, and similar high-tech digital technologies. Successful candidates will have a background in mathematics, physics, computer science or engineering. Although qualification to PhD level is preferred, we will consider any candidate with a strong first or further degree who demonstrates the required skill and knowledge to handle these technologies. Experience, Skills & Qualifications You will be comfortable working in a modern, fast-paced environment where you are given a level of autonomy to do your work. Successful candidates will also be able to demonstrate the following: Excellent academics An appropriate professional attitude (personable, well prepared, flexible and enthusiastic) Excellent written and oral communication skills Ability to express complex ideas clearly and concisely, and the ability to structure a precise and coherent argument Ability to deal with a variety of people at different levels Ability to balance knowledge of intellectual property law against commercial requirements Ability to work under pressure, which may be the result of competing and inflexible deadlines when working for more than one client at the same time Excellent research and presentation skills Meticulous attention to detail, and an analytical mind Initiative and the ability to act independently and manage own workload About EIP EIP is award-winning patent firm which and specialises in high-value and complex patent matters. In 2024 EIP won Managing IP’s ‘European Patent Contentious Firm of the Year’ award and for the sixth year in a row. EIP has been ranked in the FT's list of Europe’s Leading Patent Law Firms and is one of only three firms in Europe to achieve a gold ranking in each of their six categories. EIP has around 185 employees who operate from six European offices (London, Bath, Leeds, Cardiff, Stockholm and Düsseldorf) as well as one office in the US (Denver). Our multidisciplinary team combines patent attorneys, litigators and commercial IP lawyers, has an impressive global client base from SMEs to multinational blue-chip companies and includes telecoms owners, major software developers, pharma and biotech companies, medical device manufacturers, aerospace and logistics companies. Diversity is an intrinsic part of EIP’s business culture. We are proud to support the IP Inclusive initiative, and we are a signatory to the IP Inclusive Charter. EIP actively engages in diversity efforts and is committed to developing an attitude of openness for the benefit of all those working in the IP profession. Other Information With our state-of-the-art tech platform, we offer hybrid working, three days in the office and two from home. EIP’s employees also enjoy reduced business hours on the days when working from the office subject to there being no urgent work commitments. EIP has a friendly, progressive and mutually supportive working environment along with a smart casual dress policy and stylish modern offices. Show more Show less

33184BR Bangalore - Campus Job Description Position Summary: We are seeking an experienced ServiceNow Architect to lead the design, development, and implementation of ServiceNow solutions tailored to the needs of the telecom industry. The ideal candidate must have deep knowledge of ServiceNow modules, telecom business processes, and industry-specific requirements. They will collaborate with cross-functional teams to align ServiceNow capabilities with strategic business objectives. Key Responsibilities Develop, Review, Implement scalable ServiceNow architecture for telecom operations. Design workflows, data models, and configurations tailored to telecom processes (e.g., order management, service assurance, network operations). Ensure alignment with industry standards and best practices. Lead the implementation of key ServiceNow modules, including ITSM, ITOM, CSM, FSM, and Telecom Service Management (TSM). The candidate should have to build customized business flows in ServiceNow. Keep exploring new features and look for the opportunity to apply to make the platform robust and user friendly. Integrate ServiceNow with 3rd party applications using APIs. Collaborate with business units to gather requirements and translate them into technical solutions. Act as a trusted advisor to business and IT stakeholders, providing guidance on ServiceNow capabilities. Provide technical leadership to developers and administrators. Conduct code reviews, ensure best practices, and mentor team members on ServiceNow development. Monitor and optimize ServiceNow performance, ensuring high availability and efficient processing. Manage platform upgrades and patch implementations. Establish/Improve governance frameworks for the ServiceNow platform. Ensure compliance with regulations, data privacy, and security standards. Key Skills & Qualifications Extensive experience with ServiceNow platform architecture and development including ATF. Proficiency in scripting (JavaScript, AngularJS) and integrations using APIs, REST, SOAP. Hands-on experience with telecom modules like Telecom Service Management (TSM) is a plus. In-depth understanding of telecom operations, including OSS/BSS, network inventory management, service provisioning, and fault management. ServiceNow Certified Implementation Specialist and System Administrator (preferred). 10+ years of overall and 5+ years ServiceNow experience with at least 3+ years in an architect role. Prior experience working in the telecom sector is highly desirable. Strong problem-solving and analytical skills. Excellent communication and stakeholder management abilities. Ability to lead cross-functional teams and manage complex projects. Qualifications Bachelor in Computers Range of Year Experience-Min Year 10 Range of Year Experience-Max Year 18 Show more Show less

33298BR Chennai Job Description Roles and Responsibilities Guide delivery teams based on project needs Ensure the delivery chain executes smoothly Ensure construction of software adheres to the handbooks and best practices Drive and analyse client and end-user feedback to discover opportunities to improve the overall user experience throughout the design process and product lifecycle Work directly with client stakeholders and end-users to design end-to-end experiences using participatory and iterative design techniques including observational studies, user interviews, usability testing, and other forms of qualitative and quantitative research to uncover insights, learn about user behaviour and verify design concepts Execute full software development life cycle right from requirement gathering till production support Design, develop, implement and maintain BPM/CRM application software using PEGA platform Lead development team and coordinate with developers at different delivery centres across the globe Verify all functional and technical requirements are covered in completed technical designs and build Work with users/servicing team to build a solution that improves servicing capability and productivity Qualifications M.Sc., MCA., BE., Range of Year Experience-Min Year 5 Range of Year Experience-Max Year 7 Show more Show less

33297BR Chennai Job Description Roles and Responsibilities Guide delivery teams based on project needs Ensure the delivery chain executes smoothly Ensure construction of software adheres to the handbooks and best practices Drive and analyse client and end-user feedback to discover opportunities to improve the overall user experience throughout the design process and product lifecycle Work directly with client stakeholders and end-users to design end-to-end experiences using participatory and iterative design techniques including observational studies, user interviews, usability testing, and other forms of qualitative and quantitative research to uncover insights, learn about user behaviour and verify design concepts Execute full software development life cycle right from requirement gathering till production support Design, develop, implement and maintain BPM/CRM application software using PEGA platform Lead development team and coordinate with developers at different delivery centres across the globe Verify all functional and technical requirements are covered in completed technical designs and build Work with users/servicing team to build a solution that improves servicing capability and productivity Qualifications M.Sc., MCA., BE., Range of Year Experience-Min Year 5 Range of Year Experience-Max Year 7 Show more Show less