BULK hiring!! * Handle Queries, Requests and Complaints from customers by ensuring end to end resolution. * Ensure a significant improvement in customer experience. 5 days working Excellent English Communication skill Required Candidate profile Grad/PG Rotational Shifts Fresher / Experience Immediate joiners Candidate must be available for face to face round of interview .Unlimited incentives. Allowance.

BULK HIRING for International process!! Resolve customer's queries & complaints. Build sustainable relationships and trust with customer Excellent Communication Required Candidate profile Mohali/Chandigarh Qualification - 12/Grad/PG Rotational Shift Fresher / Experience Immediate joiners Candidate must be available for face to face interview

MASS HIRING for Freshers/Experienced !! Resolve customer's queries & complaints. Build sustainable relationships and trust with customer 5 days working with cab services. GREAT Incentives Cab facility Required Candidate profile Excellent English Communication required UG/Grad/PG Fresher/Exp. Rotational Shifts ( 24*7) Immediate joiners only Candidate must be available for face to face round of interview .5 days working

BULK HIRING!! International Chat/Voice/Blended:- # Solve customer problems, answer questions & provide support # Provide accurate and up-to-date information about products 5 days working with cab Work From Office Required Candidate profile Qualification - 12/Grad/PG Rotational Shifts Fresher /Experience Immediate joiners Candidate must be available for face to face round of interview .Unlimited incentives. Allowance. Bonus. Cabs.

Handle Queries, Requests and Complaints from customers by ensuring end to end resolution. Foster strong relationships with customers Rotational shifts with 5 days working Required Candidate profile Immediate joiners Excellent communication skills Candidate must be comfortable with Rotational shifts UG/Grad/PG Fresher & Experienced both can apply Face to Face interview only

Develop and maintain interactions with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product and HEOR related questions. MSLs will use various channels for interactions (1:1, group presentation; remote, etc). Develop and execute a medical interaction plan with Key accounts (Army, Railways, CGHS etc.) as per the needs of the stakeholders and the overall medical strategy. Effectively present information to HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives. Actively assess the medical landscape by meeting with Thought Leaders to understand their needs and expertise. Continuously update their own knowledge in treatment strategies, products, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers. Collect and provide meaningful medical insights back to the medical and commercial organizations to be actioned in support of the strategy development. Report safety information, including adverse events, in accordance with BMS Standard Operating Procedures. Contribute to the Country Medical Plan Develop territory Field Medical plan and TL Interaction plans based on therapeutic area objectives and TLs needs. Execute certain medical plan activities as assigned. Adopt institution/account planning approach and contribute to cross-functional institution/account plans. Contribute to development and delivery of scientifically meaningful medical programs/projects in line with the local Medical and Field Medical plan. Provide Medical Support As necessary and appropriate, support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Market Access). Provide scientific support at promotional meetings by presenting unbiased scientific and clinical data, by evaluating speakers and by giving support to BMS-contracted speakers. Support Clinical Trial Activities Support Interventional and Non-Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with local medical management and as defined by the study scope document. Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with local medical management. Actively support CRO sponsored studies as agreed with local medical management and as defined by the study scope document. Support HCPs in the ISR submission process as agreed with local medical management. Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events. Contribute towards the Patient advocacy programs Support the implementation of the patient education programs in collaboration with the patient advocacy groups. Support the creation of patient education materials. Report safety information, including adverse events, in accordance with BMS Standard Operating Procedures Qualifications MBBS, MD, BDS, MDS 1-2 years of Field Medical experience in medical affairs is preferred. Candidates with experience in the Oncology and Haematology therapy area will be preferred. Languages Excellent English language skills - spoken and written. Experience And Knowledge Working in a scientific and/or clinical research environment Ability to work independently and act as a team player. Have an innovative mindset and approach. Translating scientific or clinical data into an understandable and valuable form to help physicians best serve their patients. Good communication and presentation skills to present scientific and/or clinical data to research or healthcare professionals Developing peer-to-peer relationships with TLs, scientists and other healthcare professionals Ability to quickly and comprehensively learn about new subject areas and environments. Disease area knowledge and an understanding of scientific publications Knowledge of clinical trial design and process Knowledge of the national healthcare and access environment Knowledge of HEOR core concepts (Health economic and outcome research) is a plus.

The overall purpose and main responsibilities are listed below: Contribute at different levels in execution of assigned Evidence Synthesis projects (including but not limited to search strategy development, screening, data extraction) to generate robust evidence to maximize the value propositions in support of programs/products for Global/Local markets Seek opportunities to innovate HEVA value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA evidence to ensure reimbursement decisions optimal access Develop and maintain TA expertise People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA teams across various time zones Performance: (1) Contribute at different levels in execution of assigned Evidence Synthesis projects (including but not limited to search strategy development, screening, data extraction): Support activities for research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (2) Support execution of approved HEVA study(s) and manage ongoing study(s) if required: Supports the manager/HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products; Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes (3) Support development of core value dossier (CVD) and AMCP dossiers and provide strategic direction Process: (1) Assist HEVA team in development of HEVA strategic evidence material (2) Contribute in development of core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (3) Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes Stakeholder: (1) Work with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables (2) Assist HEVA team to prepare relevant & customized deliverables for these Teams About you Experience: 3+ years of experience in HEOR for the pharmaceuticals industry, CRO consultancy or academia. Soft skills: Stakeholder management; writing/communication skills; external engagement and ability to work independently and within a team environment Technical skills: Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree Languages: Excellent knowledge of English language (spoken and written)

The overall purpose and main responsibilities are listed below: Support Manager/Team Lead in execution of assigned Evidence Synthesis projects (including but not limited to search strategy development, screening, data extraction, report writing) to generate robust health economics and value based evidence to maximize the value propositions in support of programs/products for Global/Local markets Support the execution of quality research projects, economic models, trial design recommendations and other activities in support of programs/products Seek opportunities to innovate HEVA value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA evidence to ensure reimbursement decisions optimal access Develop and maintain TA expertise People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA teams across various time zones Performance: (1) Support Manager/Team Lead in execution of assigned Evidence Synthesis projects (including but not limited to search strategy development, screening, data extraction, report writing): Develop research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide strategic support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (2) Support execution of approved HEVA study(s) and manage ongoing study(s) if required: Supports the manager/HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products; Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes (3) Support development of core value dossier (CVD) and AMCP dossiers and provide strategic direction Process: (1) Assist in development of HEVA strategic evidence material (2) Assist manager in development of core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (3) Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes Stakeholder: (1) Work with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables (2) Support HEVA team to prepare relevant & customized deliverables for these Teams About you Experience: 5+ years of experience in HEOR for the pharmaceuticals industry, CRO consultancy or academia. Soft skills: Stakeholder management; writing/communication skills; external engagement and ability to work independently and within a team environment Technical skills: Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies; Understands reimbursement decisions to determine value drivers and how evidence is used in decision making and how it impacts various payers (e.g., providers, patients, health systems); Knowledge of methods and principles of health economics, health technology assessment (HTA) reviews Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree

* Resolve client queries & assess their needs to achieve satisfaction. * Build sustainable relationships and trust with customer 5 days working with cab services. Required Candidate profile Qualification - 12/Grad/PG Rotational Shift Fresher / Experience Immediate joiners Candidate must be available for face to face round of interview .5 days working EPF/ESI Incentives cabs

The overall purpose and main responsibilities are listed below: Assist HEVA team in assigned therapy area portfolio to plan and generate robust health economics and value based evidence to maximize the value propositions from both a global and US perspective working within the Market Access tripod Contribute to the execution of quality research projects, economic models, trial design recommendations and other activities in support of programs/products Seek opportunities to innovate HEVA value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA evidence to ensure reimbursement decisions optimal access Develop and maintain TA expertise People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA teams across various time zones Performance: (1) Contribute in the HEVA evidence generation plan: Support activities for research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (2) Support execution of approved HEVA study(s) and manage ongoing study(s) if required: Supports the manager/HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products; Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes (3) Support development of core value dossier (CVD) and AMCP dossiers and provide strategic direction Process: (1) Assist HEVA team in development of HEVA strategic evidence material (2) Contribute in development of core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (3) Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes Stakeholder: (1) Work with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables (2) Assist HEVA team to prepare relevant & customized deliverables for these Teams About you Experience : 5 + years of experience in HEOR for the pharmaceuticals industry, CRO consultancy or academia. Soft skills : Stakeholder management; writing/communication skills; external engagement and ability to work independently and within a team environment Technical skills : Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies Education : Advanced degree in life sciences/pharmacy/similar discipline or medical degree Languages : Excellent knowledge of English language (spoken and written)

Job Title: Senior SEO Expert Location: Infopark, Kochi Company: NewAgeSysIT About Us: NewAgeSysIT, a division of NewAgeSys, Inc. (est. 1994), is a fast-growing digital solutions company based in Princeton, NJ. We serve global clients across industries like healthcare, logistics, education, and more. Role Overview: We re looking for a results-driven Senior SEO Expert to lead our organic growth and lead generation efforts. You ll work closely with content, development, and marketing teams to execute effective SEO strategies. Key Responsibilities: Conduct keyword research and optimize web content Implement On-page, Off-page, and Technical SEO best practices Collaborate with developers on site performance and Technical SEO Build backlinks and manage Off-page strategies Track performance metrics and generate SEO reports Guide and mentor junior team members Requirements: 3+ years of hands-on SEO experience Strong knowledge of SEO tools (GA, Search Console, Ahrefs, etc.) Familiarity with WordPress, HTML/CSS/JS, and CMS platforms Excellent analytical and leadership skills Bonus Skills: Local SEO, schema markup, CRO, and content marketing experience Why Join Us Work with a global team on cutting-edge projects Flexible work setup Opportunity to lead and grow a team <

Opening for Freshers and Experience candidates in BPO Domain for Customer Support English + Tamil required Salary 14k to 25k Inhand Walk-in Interviews Providing customer support. Work Location :Chennai, Bangalore, Hyderabad -Language- English+ Tamil -Graduation not mandatory. -Immediate joiners required. Voice Process / Non voice / Call center / BPO Pls call Niveda 9884676582 for more info Thanks, Niveda 9884676582

Hiring for Leading ITES Company In Gurgaon/Noida for Customer Support Requirements: Min 1 Year BPO/Customer Service Experience Daily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3) Landmark : Near Hotel Nirulas Walkin Time : 11 am to 4 Pm Whatsapp Your CV @ 9721919721 Job Details: 1: Graduate/UG With Min 1 Year Exp in Customer Support 2: Candidate Must Not Have Any Exams in the Next 6 Months 3: Rotational Shifts 4: Customer Support 5: 5 Days Working 6: Max 5.8 LPA 7: Excellent Communication Skills 8: Immediate Joiners Preferred

Were looking for a passionate and driven Business Development Manager (Pharmacovigilance) to join our expanding team! This role focuses on managing client relationships at the mid-to-senior level, driving new business acquisition, expanding existing accounts, ensuring client satisfaction, and maintaining strong, strategic partnerships. Key Responsibilities Proactively identify and pursue new business opportunities within the assigned territory to develop new client accounts. Meet or exceed sales and business development goals by designing and executing effective go-to-market strategies for targeted industries and clients. Generate a pipeline of qualified sales leads and RFPs by engaging in strategic prospecting aligned with client budget cycles, timelines, and decision-making frameworks. Participate in the full business development lifecycle including RFP/RFI submissions, pricing negotiations, proposal creation, and contract execution. Build and maintain lasting relationships with key client stakeholders and gain a deep understanding of their business needs to uncover opportunities for collaboration. Develop and manage a detailed sales plan for the assigned region and accounts, ensuring that tailored solutions and strategies align with client expectations. Oversee proposal development processes, ensuring alignment between client expectations and internal capabilities, timelines, and budgets. Act as the primary point of coordination between clients, partners, and internal delivery teams to ensure smooth execution and communication. Maintain accurate records of sales activities in the CRM system and regularly present activity and pipeline reports to sales leadership and business heads. Demonstrate strong verbal and written communication skills, with the ability to influence and collaborate effectively. Represent Clinevo at global conferences, meetings, and industry forums. Job Qualification: A minimum of 5 years of successful sales and business development experience within a Clinical Research Organization (CRO), with established industry networks. Proven expertise in promoting pharmacovigilance (drug safety) and other CRO-related services or Life Sciences Sales. Deep understanding of drug safety and regulatory needs. Strong negotiation and consultative sales skills. Solid understanding of CRO operations and client relationship dynamics. Bachelor's degree in Pharmacy (B. Pharm) or Master's in Pharmacy (M. Pharm) is required; an MBA is a plus. A strong network in life sciences, biotech, or pharma. A proactive, entrepreneurial spirit with a focus on results. Location & timings This is a full-time in-person role with the office based in Bengaluru. Working pattern & hours are Monday - Friday, 40 hours per week. The timings typically would be US EST time zone but we could align once you onboard. Compensation & Benefits Competitive salary with performance-based incentives. Rapid career growth in a high-impact role A collaborative and supportive culture Why join us? At Clinevo , we believe that advancing drug safety means pushing boundaries — together. If you’re ready to accelerate your career and make a real difference, we want to hear from you! Our values shape our corporate culture and distinguish us from the competitors. They support our purpose and give us guidance - everyday.

Fresher or minimum 6 months experience in International voice process is required with papers, Graduation mandatory. Excellent communication required. Night shift, 2 days rotational off. Candidates have to collect system from Mumbai or Gurgaon office. BPO for Customer support Voice process. Work location - Only Mumbai & Gurgaon. Work from Home. Candidates have to collect system from Mumbai or Gurgaon office. Telephonic interview will be done. Immediate joining is required. Excellent communication req Sal 2 lpa to 2.5 lpa. 2 days rotational off Graduation mandatory. Sal upto 4.5 lpa. Immediate joining required. Pls read the above job description and if your profile matches the requirement, pls call the given no Please apply for the job in Naukri.com. We will check & will update you. Do not search the number in Google and do not call us. The requirements are not yet active from Client's side.

Fresher or minimum 6 months experience in International voice process is required with papers, Graduation mandatory. Excellent communication required. Night shift, 2 days rotational off. Candidates have to collect system from Mumbai or Gurgaon office. BPO for Customer support Voice process. Work location - Only Mumbai & Gurgaon. Work from Home. Candidates have to collect system from Mumbai or Gurgaon office. Telephonic interview will be done. Immediate joining is required. Excellent communication req Sal 2 lpa to 2.5 lpa. 2 days rotational off Graduation mandatory. Sal upto 4.5 lpa. Immediate joining required. Pls read the above job description and if your profile matches the requirement, pls call the given no Please apply for the job in Naukri.com. We will check & will update you. Do not search the number in Google and do not call us. The requirements are not yet active from Client's side.

Hiring Freshers Good Communication Flexibility to work in Night Shifts Graduates (Arts/ Life Science / Commerce /Business Administration) only can apply Graduated Year 2019 - 2024, No backlogs Note: B.E & B. Tech graduates are not eligible

Roles and Responsibilities: Provides Qualifications and Agreements by: Maintaining current, up-to-date curriculum vitae. Maintaining current licensure to practice. Demonstrating the proper education, training and experience to conduct the clinical investigation. Assuming responsibility for the conduct of the clinical investigation. Ensures Protocol Compliance by: Possessing a thorough understanding of the requirements of each protocol. Determining that inclusion / exclusion criteria are applicable to the study population. Ensuring recruitment goals are reasonable and attainable. Reviewing the inclusion / exclusion criteria, schedule of visits, end point criteria and investigational article use with the research team. Manages the Medical Care of Subjects by: Assessing subject compliance with the test product and follow-up visit. Assessing subjects response to therapy. Evaluation of adverse experiences. Ensuring that medical care is provided to a subject for any adverse event(s) that is reported. Informing a subject when medical care is needed to treat an inter-current illness(es). Protects the Rights and Welfare of Subjects by: Ensuring that the informed consent form contains all the elements required. Obtaining a signed and dated informed consent from the subject or subjects legal representative prior to initiation of any study-related procedures. Informing the subject or legal representative about all aspects of the clinical trial. Ensures Documentation of Study-Related Procedures, Processes and Events by: Conduction of physician examination as per the protocol and applicable procedures for volunteers. Documenting deviations from the approved protocol. Documenting that informed consent has been obtained from the subject or legal representative. Documenting adverse event(s). Complying with written procedures to document changes to data and / or case report forms. Maintaining trial documents as required by the regulations and sponsor for the appropriate timeframe and under secure conditions. Maintains Professional and Technical Knowledge by: Attending education workshops. Reviewing professional publications. Participating in professional societies. Other responsibilities as assigned by the DGM-Clinical Operations / Principal investigator from time to time. Desired Candidate Profile can send to email: hr@qpsbioserve.com Note: Opening for 2 Male physician

Captive Unit Customer Service - Voice Process - Gurgaon Location Excellent Communication (Versant Round) 24*7 Shifts AGE LIMIT - 30 yrs MAX Salary Max 4.50 Lacs (Take Home - 33k) Share resume at mohan@marvelplacements.com or Call @ 9958521703 Required Candidate profile Captive Unit Customer Service - Voice Process - Gurgaon Location AGE LIMIT - 30 yrs MAX Share resume at mohan@marvelplacements.com or Call @ 9958521703

Captive Unit Customer Service - Voice Process - Gurgaon Location Excellent Communication (Versant Round) 24*7 Shifts AGE LIMIT - 30 yrs MAX Salary Max 4.50 Lacs (Take Home - 33k) Share resume at mohan@marvelplacements.com or Call @ 9958521703 Required Candidate profile Captive Unit Customer Service - Voice Process - Gurgaon Location AGE LIMIT - 30 yrs MAX Share resume at mohan@marvelplacements.com or Call @ 9958521703

Hiring for Leading ITES Company In Gurgaon/Noida for Customer Support Requirements: Min 1 Year BPO/Customer Service Experience Daily Walkin @ Outpace Consulting, C-29, Sec 2 Noida (Nearest Metro Noida Sec 15, Exit Gate 3) Landmark : Near Hotel Nirulas Walkin Time : 11 am to 4 Pm Whatsapp Your CV @ 9721919721 Job Details: 1: Graduate/UG With Min 1 Year Exp in Customer Support 2: Candidate Must Not Have Any Exams in the Next 6 Months 3: Rotational Shifts 4: Customer Support 5: 5 Days Working 6: Max 5.8 LPA 7: Excellent Communication Skills 8: Immediate Joiners Preferred

International process- VOICE/ CHAT !! # Handle customer complaints, queries. # Provide appropriate solutions and alternatives. CAB facilities with 5 days working Call/WhatsApp HR Priyanka @ 7037375529 . Required Candidate profile Excellent English Communication Location- Mohali/ Chandigarh UG/Grad/PG Fresher/Exp. Rotational Shifts WORK FROM OFFICE Immediate joiners Candidate should be comfortable for face to face interview. Perks and benefits 5 Day working Cabs Unlimited Incentives Epf

ql-editor "> Job Summary: The QC Reviewer is responsible for ensuring the accuracy, completeness, and compliance of laboratory and clinical data with regulatory guidelines, company policies, and industry standards. This role is critical in maintaining the integrity of research conducted within the organization, ensuring adherence to Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) guidelines. Key Responsibilities: Review raw data, study documentation, analytical reports, and other records to ensure accuracy and compliance with regulatory standards (FDA, EMA, ICH, etc.). Verify data integrity, consistency, and adherence to protocols, standard operating procedures (SOPs), and regulatory requirements. Ensure proper documentation practices (ALCOA+ principles) are followed in all QC-reviewed data. Identify discrepancies, deviations, and errors in reports and provide recommendations for corrective actions. Collaborate with laboratory analysts, study coordinators, and quality assurance teams to resolve issues related to data accuracy and compliance. Maintain proper documentation of QC reviews and findings, preparing detailed reports for management and regulatory bodies as required. Participate in audits (internal and external) and inspections by regulatory authorities. Provide training and mentorship to junior QC staff and other relevant team members on compliance and quality standards. Stay updated with regulatory changes and industry best practices to enhance the organization s quality standards. Qualifications Experience: Bachelor s/Master s degree in Life Sciences, Pharmacy, Chemistry, or a related field. 2-6 years of experience in a Quality Control/Quality Assurance role within a Contract Research Organization (CRO), pharmaceutical, or biotech industry. Strong knowledge of GLP, GCP, FDA, EMA, and ICH guidelines. Proficiency in reviewing analytical data, clinical study reports, and laboratory documentation. Excellent attention to detail and problem-solving skills. Strong communication and interpersonal skills to work effectively with cross-functional teams. Proficiency in Microsoft Office and Laboratory Information Management Systems (LIMS) is preferred. Preferred Skills: Experience with bioanalytical, clinical, or preclinical study reviews. Knowledge of electronic data capture (EDC) and regulatory submission processes. Ability to handle multiple projects with tight deadlines while ensuring compliance and accuracy.

ql-editor "> Job Summary: The Report Writer is responsible for preparing high-quality scientific and technical reports, including clinical study reports (CSRs), bioanalytical reports, and regulatory submission documents. This role ensures that all reports comply with regulatory guidelines, industry standards, and internal SOPs while effectively communicating scientific findings. Key Responsibilities: Prepare and review scientific and technical reports, including clinical study reports, bioanalytical reports, and method validation reports. Ensure clarity, accuracy, and compliance of reports with regulatory requirements (FDA, EMA, ICH, etc.) and Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) standards. Work closely with scientists, analysts, statisticians, and quality assurance teams to interpret data and ensure accurate presentation of study results. Format reports as per client specifications and regulatory submission requirements. Maintain version control and track report progress to ensure timely completion of deliverables. Perform quality control (QC) checks on reports to identify inconsistencies, errors, or deviations from standard practices. Assist in the preparation of summaries, manuscripts, and other scientific documents for publication or regulatory submission. Stay updated with regulatory guidelines, industry best practices, and emerging trends in medical and regulatory writing. Qualifications Experience: Bachelor s/Master s degree in Life Sciences, Pharmacy, Biochemistry, or a related field. 2-6 years of experience in medical writing, regulatory writing, or scientific writing within a Contract Research Organization (CRO), pharmaceutical, or biotech industry. Strong knowledge of GLP, GCP, and ICH guidelines related to clinical and bioanalytical reporting. Excellent writing, editing, and proofreading skills with high attention to detail. Ability to interpret scientific data and present it clearly and concisely. Proficiency in Microsoft Office (Word, Excel, PowerPoint) and document management systems. Strong organizational and time management skills to handle multiple projects and meet tight deadlines. Preferred Skills: Experience with regulatory submissions, clinical protocols, and investigator brochures. Familiarity with statistical concepts and data analysis tools. Knowledge of electronic submission processes and regulatory writing software.

Position Overview: We are looking for a skilled and data-driven ASO Specialist to optimize mobile apps for higher visibility, rankings, and downloads. The ideal candidate will have 1 to 4 years of experience in App Store Optimization (ASO) and a deep understanding of app store algorithms, keyword optimization, and user engagement strategies . Key Responsibilities: Develop and implement ASO strategies to increase app visibility and downloads in Google Play Store & Apple App Store . Conduct keyword research & metadata optimization to enhance search rankings. Optimize app listings, including titles, descriptions, icons, screenshots, and videos for better conversion rates. Perform A/B testing on app creatives to maximize user engagement. Monitor app performance metrics such as rankings, downloads, retention rates, and user engagement. Work closely with developers, designers, and marketing teams to align ASO strategies with overall business goals. Optimize ratings and reviews management , ensuring improved customer feedback and response strategies. Analyze competitor apps and identify industry trends to implement effective optimization techniques. Stay updated with the latest ASO trends, algorithm updates, and best practices to maintain a competitive edge. Requirements: 1 to 4 years of hands-on experience in ASO or mobile app marketing. Strong understanding of Google Play Console & Apple App Store Connect . Proficiency in ASO tools such as App Annie, Sensor Tower, Mobile Action, The Tool, or similar . Experience with keyword research, A/B testing, and conversion rate optimization (CRO) . Knowledge of mobile app analytics & user behavior tracking . Basic understanding of SEO, paid app promotion, and mobile marketing strategies is a plus. Strong analytical and problem-solving skills . Excellent communication and teamwork abilities .