510 Biostatistics Jobs - Page 7

Location: India – Remote working Type: Full time Compensation: 20 - 30 lk p.a. Are you passionate about turning real-world data into real-world outcomes? At Prospection , we empower better healthcare decisions by uncovering insights from large-scale health data sets. We’re looking for an Analytics Consultant to join our fast-growing team. This hands-on role will drive high-impact analytics projects that help pharmaceutical companies, healthcare providers, and governments improve patient outcomes—across Australia and globally. About Us Prospection is a pioneer in healthcare analytics, using machine learning and predictive modelling to analyse real-world data—claims, EMR, registries, supply chain and more. From immuno-oncology to hepatitis, our insights have supported 70+ therapy areas worldwide. What You’ll Do Support lifecycle of pharmaceutical products, from development to market launch and beyond Assist in the development and optimization of new pharmaceutical Products Conduct patient-centric analyses to gain a comprehensive understanding of the end-to-end patient journey Conduct market research to identify trends, opportunities, and competitive landscape Develop detailed understanding of key customer and industry use cases and partner with Product and Sales to prioritize features and continually improve our Data and Platforms. Work closely with the regional analytics teams and subsequently collaborating with Product team to share learnings and the solution design Support the team to work alongside product squads providing practical advice on how to productise analytics solutions within our product vision and roadmap Consistently generate innovative ideas to shape best practices for analytics and serve as a mentor for less seasoned team members Essential Criteria 3+ years’ experience in commercial data analytics, data science or manipulating and drawing insights from data. Domain knowledge within healthcare and/or epidemiology, combined with analytical expertise utilising Real World Data (RWD) Prior experience with patient data and claims data is preferred Hands-on problem-solving experience using quantitative and analytical abilities and tools, e.g., Spark, SQL, Python, R, tableau, Power BI etc. Strong interpersonal communication skills, including written, verbal, presentation etc. Tertiary qualifications in a quantitative discipline (E.g., Mathematics, Statistics, Biostatistics, Health Economics, Computer Science, Actuarial Studies, Engineering) Why Join Prospection? Impact: Work on meaningful projects that improve patient care globally Growth: Be part of a scale-up with career advancement opportunities Culture: Join a collaborative, mission-driven team passionate about healthcare and data Learning: Access a wide range of professional development and mentorship opportunities If you're ready to make a real difference with data, we’d love to hear from you. Apply now Know someone perfect for this? Share this post!

About The Job Our Team: Sanofi Global Hub is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities The Biostatistician will work with Medical Affairs biostatisticians and Sanofi Global Hub biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, and manuscripts); The Biostatistician will ensure SOPs are followed and timelines and quality metrics are met. People Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs. Performance / Process Conduct appropriate post-hoc statistical analyses of clinical trial data. Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. Produce well documented data packages that include tables, listings, and figures. Closely follow QC plans and timelines set by senior members of the Sanofi Global Hub biostatistics and programming team. Review appropriate biomedical and clinical research literature related to assigned project(s). Customer Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables. About You Experience : Master's degree with 3-6 years (M.Sc.) of experience required /Ph.D. in biostatistics or statistics or epidemiology and 2-3 years. Soft skills : Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment, High proficiency in statistical methods used in the pharmaceutical industry, Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines. Technical skills : Advance SAS programming skills, SDTM & ADaM (CDISC) and other statistical computing software skills in a clinical data environment across multiple therapeutic areas. Education : Master of Science degree or equivalent in Statistics/ Ph.D. in biostatistics or statistics or epidemiology. Languages : Excellent English language knowledge – written and spoken Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! null Pursue Progress . Discover Extraordinary . Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Develop Medical Devices Algorithm, Test Medical Devices , Clinical Trials, Patient Monitoring, FDA Applications, CE Certifications, ISO Certifications. Perform testing, calibration, troubleshooting, and repair of medical electronic equipment. Collaborate with cross-functional teams including R&D, manufacturing, quality assurance, and clinical staff to ensure product safety and effectiveness. Ensure compliance with medical device regulations and standards (e.g., FDA, IEC 60601, ISO 13485).

The Biostatistician will work with Medical Affairs biostatisticians and Sanofi Global Hub biostatistics and programming personnel to implement statistical analysis plans and provide QC d data packages including tables, figures, and listings for use in publications (i-e- abstracts, posters, oral, presentations, and manuscripts); The Biostatistician will ensure SOPs are followed and timelines and quality metrics are met- People: Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product with an objective to develop statistical data outputs- Performance / Process: 1) Conduct appropriate post-hoc statistical analyses of clinical trial data- 2) Design, develop, test, implement, and document statistical programming in high-level software packages e-g- SAS- 3) Produce well documented data packages that include tables, listings, and figures- 4) Closely follow QC plans and timelines set by senior members of the Sanofi Global Hub biostatistics and programming team- 5) Review appropriate biomedical and clinical research literature related to assigned project(s)- Customer: Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables- About you Experience : Masters degree with 3-6 years (M-Sc-) of experience required /Ph-D- in biostatistics or statistics or epidemiology and 2-3 years- Soft skills : Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment, High proficiency in statistical methods used in the pharmaceutical industry, Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines- Technical skills : Advance SAS programming skills, SDTM & ADaM (CDISC) and other statistical computing software skills in a clinical data environment across multiple therapeutic areas- Education : Master of Science degree or equivalent in Statistics/ Ph-D- in biostatistics or statistics or epidemiology- Languages : Excellent English language knowledge written and spoken

Role & responsibilities Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR); Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies; Writes code using Base SAS programs, SAS procedures, or standardized macros; Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data; Performs data checks as needed, to ensure integrity and correctness of data displays; Prepares documentation for programs; Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole; Creates SAS datasets of clinical data from clinical databases; Creates status and efficacy datasets; Creates project-specific macros and formats; Loads client data from other platforms and other software packages; Prepares data to be sent to clients and as needed for other external transfers and data imports. In addition to above job duties, SP II also Assists manager and/or director to keep track project timelines and deliverables; Leads junior programmers in daily activities and performs on-the-job training to them; Communicates with clients for risks, issues, and potential delays. Requirements 1. Ability to communicate effectively in English, in both writing and verbal. 2. Ability to learn quickly and pay attention to details. 3. Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries. 4. Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients. 5. Ability to work independently, takes ownership and strives for quality and efficiency. 6. Ability to work positively in a continually changing environment. 7. Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.

Role & responsibilities Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR); Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies; Writes code using Base SAS programs, SAS procedures, or standardized macros; Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data; Performs data checks as needed, to ensure integrity and correctness of data displays; Prepares documentation for programs; Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole; Creates SAS datasets of clinical data from clinical databases; Creates status and efficacy datasets; Creates project-specific macros and formats; Loads client data from other platforms and other software packages; Prepares data to be sent to clients and as needed for other external transfers and data imports. In addition to above job duties, SP II also Assists manager and/or director to keep track project timelines and deliverables; Leads junior programmers in daily activities and performs on-the-job training to them; Communicates with clients for risks, issues, and potential delays. Requirements 1. Ability to communicate effectively in English, in both writing and verbal. 2. Ability to learn quickly and pay attention to details. 3. Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries. 4. Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients. 5. Ability to work independently, takes ownership and strives for quality and efficiency. 6. Ability to work positively in a continually changing environment. 7. Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.

About the job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main responsibilities: The Senior Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests) ;The Senior Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques; The Senior Statistical Programmer will ensure SOPs are followed and timelines and quality are met. People: 1) Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and/or programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs. Performance / Process: 1) Conduct appropriate post-hoc statistical analyses of clinical trial data and/or registry. 2) Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. 3) Produce well documented data packages that include tables, listings, and figures. 4) Remain current on advanced programming methods Customer: 1) Work closely with Global Medical Affairs biostatisticians and/or programmers to identify statistical analysis needs and assist in developing assigned deliverables About you Experience : Master's degree minimum 4 years/B.Sc. minimum 6 years of relevant experience required Soft skills : Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment Technical skills : Advance SAS programming skills, SDTM & ADaM (CDISC) Education : Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field. Languages : Excellent English language knowledge – written and spoken Pursue Progress, discover Extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

About the job Our Team: Sanofi Global Hub is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Global Hub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main responsibilities: The Biostatistician will work with Medical Affairs biostatisticians and Sanofi Global Hub biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, and manuscripts); The Biostatistician will ensure SOPs are followed and timelines and quality metrics are met. People: Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs. Performance / Process: 1) Conduct appropriate post-hoc statistical analyses of clinical trial data. 2) Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. 3) Produce well documented data packages that include tables, listings, and figures. 4) Closely follow QC plans and timelines set by senior members of the Sanofi Global Hub biostatistics and programming team. 5) Review appropriate biomedical and clinical research literature related to assigned project(s). Customer: Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables. About you Experience : Master's degree with 3-6 years (M.Sc.) of experience required /Ph.D. in biostatistics or statistics or epidemiology and 2-3 years. Soft skills : Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment, High proficiency in statistical methods used in the pharmaceutical industry, Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines. Technical skills : Advance SAS programming skills, SDTM & ADaM (CDISC) and other statistical computing software skills in a clinical data environment across multiple therapeutic areas. Education : Master of Science degree or equivalent in Statistics/ Ph.D. in biostatistics or statistics or epidemiology. Languages : Excellent English language knowledge – written and spoken Better is out there. Better medications, better outcomes, better science. But Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Job Title: Associate Director Statistical Programming Work Location: Manyata Tech Park, Bangalore, India Work Schedule: Three days on-site, two days remote (3/2) Career Level: E Individual Contributor position Introduction to role The Associate Director of Statistical Programming will oversee statistical programming activities for multiple clinical studies, maintain programming infrastructure, and ensure compliance with SOPs to produce quality and timely deliverables This role requires extensive experience and proven skills in the use of SAS within a Statistical Programming environment, along with a complete understanding of statistical programming processes, procedures, and roles The successful candidate will support Biostatistics in statistical analysis, including generating analysis data listings, tables, and figures, and creating all files necessary to support an electronic submission in the eCTD format Additionally, strong people management and supervisory skills are essential to provide direct line management to statistical programmers, identify training needs, and optimize staff utilization The role also involves managing the day-to-day activities of external partners in delivering program deliverables Accountabilities Serve as the Lead Programmer and Manager of the statistical programming efforts Develop and validate technical programming specifications for analysis datasets using Alexion or ADaM standards Independently develop and validate programs that generate analysis datasets based on Alexion or ADaM specifications Develop and validate technical programming specifications for protocol-specific efficacy tables, listings, figures/graphs Independently develop and validate programs that generate protocol-specific efficacy tables, listings, figures/graphs using Alexion specifications Ensure that the filing of study documentation is maintained to the standard required according to processes and acceptable for audit Directly support the Clinical and Statistical Programming Director in all aspects of the management and development of the Statistical Programming team Participate in the ongoing review of the processes used by the Statistical Programming group to ensure processes are continually complied with and updated as necessary Create and/or review programming plans, and ensure appropriate resource allocation and prioritization Act as the primary department contact to ensure that department standards are implemented in all studies Manage adherence to all company policies, SOPs, and other controlled documents; ensure all programming activities adhere to departmental standards Collaborate closely with Biostatistics, Clinical Data Management, Pharmacovigilance, Clinical Operations, and other functions within Alexion to address their needs for programming support Essential Skills/Experience 7+ years statistical programming experience in the CRO or Pharmaceutical Industry 4+ years project management experience in the CRO or Pharmaceutical Industry Experience with CDISC SDTM and ADaM models and transforming raw data into those standards Strong people management skills and supervisory skills gained from direct line management or supervisory experience Proven abilities to lead and manage cross-functional projects, and people, from concept to completion Strong verbal and written communication skills ability to clearly and effectively present information An excellent understanding of the roles and responsibilities of all related disciplines, in particular Biostatistics, Clinical Data Management, and Pharmacovigilance Advanced knowledge of SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, and SAS/SQL in a windows environment with a demonstrated mastery of SAS/STAT procedures Extensive experience and proven skills in the use of SAS within a Statistical Programming environment to develop and validate analysis datasets, tables, listings, and figures/graphs Knowledge of clinical database design, specifically electronic data capture using Inform, Medidata, and Oracle Advanced experience with: Constructing technical programming specifications Relational Databases Good Clinical Practices Good Programming Practices 21CFR Part 11 Standards Integrated Summary Safety/Efficacy Analyses Creating all files necessary to support an electronic submission in the eCTD format Desirable Skills/Experience BS/MS/MA in Statistics, Biostatistics, Computer Science, Mathematics or related area Competencies: Accountability Collaboration Decision Quality Drive for Results Perseverance Problem Solving Informing Peer Relationships Time Management Building Effective Teams Managing Through Systems At AstraZeneca's Alexion division, we are driven by our passion for making a difference in the lives of patients with rare diseases Our unique approach combines the agility of a biotech with the resources of a global biopharma leader We foster an inclusive culture where innovation thrives, empowering our employees to grow both personally and professionally Join us to be part of a team that is dedicated to transforming lives through groundbreaking science and compassionate care Ready to make an impactApply now! Date Posted 20-May-2025 Closing Date 30-Jul-2025 Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law Alexion provides reasonable accommodations to meet the needs of candidates and employees To begin an interactive dialogue with Alexion regarding an accommodation, please contact accommodations@Alexion, Alexion participates in E-Verify

As a Field Bioinformatics Scientist at MGI, you will play a crucial role in designing, developing, optimizing, and maintaining in-house bioinformatics pipelines and various genomics applications. Your responsibilities will include understanding customer research questions, providing tailored solutions, and addressing technical issues from global sales and customers. You will collaborate with various teams such as FAS, FSE, Product Managers, and R&D to provide feedback, develop customized solutions, and support solution provision. Your role will also involve staying updated on sequencing, bioinformatics, MGI products, and industry trends, evaluating new software/tool suitability for different applications, and applying best-practice statistical and computational methods. Additionally, you will be responsible for providing technical pre-sales and post-sales support services, conducting training sessions and webinars for customers and the front-end sales team, and managing documentations such as training materials, FAQs, slides, videos, SOPs, and knowledge base content. The ideal candidate for this position should hold a Bachelor's degree or higher with at least 3 years of experience in academic or industrial settings in Bioinformatics, Computational Biology, Biostatistics, or Computer Science. You should have expertise in developing next-generation sequencing data analysis methods for DNA, RNA, and Long read analysis, along with proficiency in scripting languages like Python, bash, Perl, C++, and R. Excellent communication skills, the ability to work independently and collaboratively, manage tasks efficiently, and adapt to a fast-paced environment are essential for this role. Experience with version control systems such as Git, a wide range of bioinformatics tools, and proficiency in Linux operating systems like Ubuntu, Fedora, CentOS, etc., will be advantageous. At MGI, we believe in promoting advanced life science tools for future healthcare and transforming lives for the better. We encourage innovation, bold decision-making, and a commitment to improving the world we live in. Join us in leading life science innovation and contributing to a healthier and longer life for everyone. With a focus on transparency, fairness, and a friendly environment, we value our employees as partners and prioritize their physical and mental well-being. Embrace our agile management approach, enjoy independence with guidance, and foster a balanced life-work culture as we strive towards a brighter and more equal future together. #Omicsforall,

Fueling Brains is a growing, vibrant organization poised to change the narrative of Education. We are looking for individuals who are passionate about transforming the world of education through a holistic, whole-brain approach to the development of young children. Children impacted by our program will grow into well-rounded, well-regulated, and joyful adults who serve their community and shape the future. We bring together the best of educational science, technology, and childcare expertise to unveil the child's infinite potential. We are looking for a Senior Neuropsychology Research Associate with a solid background in Clinical Psychology or Neuroscience to drive our research and development initiatives. This role will support product innovation, research-led strategy enhancement, and AI-powered automation of developmental data. The ideal candidate should bring in-depth knowledge of research methodologies, modern interventions, and biostatistics, with at least one research publication being a strong advantage. Key Responsibilities Lead the audit and analysis of classroom data related to brain-based activities and outcomes. Partner with academic coaches and stakeholders to interpret child development progress and implement neuroscience-driven strategies. Oversee the mapping of developmental strategies to learning activities. Collaborate with the Application Development Team for enhancements to neuroscience-based products. Conduct literature reviews and produce research-backed recommendations for curriculum and program development. Prepare Brain Map reports and assist in data consolidation for AI model training. Supervise and review periodic activity audits to ensure alignment with neuroscience frameworks. Qualifications & Skills Master’s degree in Clinical Psychology or Neuroscience (mandatory). 1–2 years of experience in a research or applied psychology environment. Strong proficiency in research methodology and basic biostatistics. Excellent communication and scientific writing skills. Demonstrated ability to interpret and apply scientific data in practical settings. Proficient with both conventional and modern computing systems. Experience or familiarity with AI applications in education or healthcare is a plus. Preferred At least one research publication in a relevant field. Knowledge of modern neuroscience interventions used in child development. Experience in cognitive or behavioral developmental frameworks. Work Environment Requirements Full-time, on-site role based in Chennai, India. Must be able to collaborate with interdisciplinary teams including Product, Data Science, and Curriculum Design. Willingness to operate in a fast-paced and research-intensive environment.

As a Biostatistician at CPVIA, a clinical data analytics solutions company in Hyderabad, you will utilize your expertise in statistical programming and consulting to support pharmaceutical, biotechnology, and medical device companies. Your primary focus will be on accelerating drug development activities while maintaining high quality standards and cost efficiency through collaboration with a team of experienced professionals. With a minimum of 3 years of experience in the pharmaceutical industry, you will play a crucial role in providing internal statistical support by closely working with lab scientists, technicians, statisticians, and programmers. Your responsibilities will involve collaborating with various stakeholders to facilitate drug development activities and ensure successful project outcomes. To excel in this role, you are required to hold a university degree in Sciences or Engineering, with a post-graduate qualification in Biostatistics or equivalent statistical experience. You should have a strong grasp of statistical theory, diverse methodologies, and experimental designs. Proficiency in SAS, R (and JMP) is essential, along with effective communication skills to bridge theoretical concepts with practical applications. Being a team player is vital as you will be expected to share knowledge within multidisciplinary teams and contribute to study oversight and delivery. Experience in developing protocols, Statistical Analysis Plans (SAP), Tables, Figures, and Listings (TFL) is advantageous. Additionally, your technical skills in power calculation, simulations, and Quality Data Model (QDM) will be valuable assets in this role. If you meet the qualifications mentioned above and are passionate about making a meaningful impact in drug development, we encourage you to apply by submitting your resume to info@cpvia.com. Join us at CPVIA and be part of a dynamic team dedicated to driving innovation and excellence in clinical data analytics.,

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials. Job Summary Apply a high level of technical expertise to help guide and develop the more junior biostatistics staff members. Serve as a lead statistician on clinical studies and provide senior level peer review of work being accomplished by other biostatisticians in the department. Maintain the statistical and analytical integrity of clinical trials analyzed by SDC. Actively participate in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, interpreting analysis results, writing statistical sections of clinical study reports, and participating in meetings with drug regulatory agencies as required. Support business development and project management with strategic planning, proposals, pricing, and timeline planning. Primary Responsibilities Serve as an internal consultant for biostatistics analysis tools and methods Serve as a subject matter expert during client and vendor meetings for biostatistics analysis support Actively support business development in capabilities presentations to prospective and current clients Effectively manage assigned clinical study budgets for biostatistics analysis support Develop, coach and mentor junior biostatistics department personnel Act as the lead statistician on clinical research projects and help with SAS programming Provide statistical expertise for study design of clinical trial protocols Write statistical methods section of the study protocol, as needed Write statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed Review CRFs to ensure consistency with protocol and statistical analysis plan (SAP) Program summary tables, data listings and graphical representations of clinical trials data Perform all analyses defined in the statistical analysis plan as well as any post-hoc analyses and relevant exploratory analyses of clinical trial data Prepare/review key sections of clinical study reports and various regulatory documents Perform statistical QC of all department outputs including analyses and clinical study reports Provide statistical support to answer questions from external clients (such as FDA, Investigators) Contribute to the development, maintenance, and training of standard operating procedures (SOPs) Represent the biostatistics department at regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed Manage biostatistics timelines, budgets, and client expectations Adhere to all aspects of the Statistics & Data Corporation's quality system Comply with Statistics & Data Corporation's data integrity & business ethics requirements Perform other related duties incidental to the work described herein Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified. Requirements Required Skills Effective leadership, budget forecast and implementation skills Excellent analytical skills, with the ability to process scientific and medical data Able to work independently and in teams Project management abilities including analytical evaluation, organization, delegation, flexible team management, negotiating and resource management skills Excellent knowledge of statistical programming Expertise in manipulating and analyzing SAS data Able to identify data issues, present problems, and implement solutions Capable of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues and clients Excellent organizational and time management skills, with the ability to multi-task Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP) Strong interpersonal communication and presentation skills Able to effectively collaborate across cross-functional teams Focus on quality at all times and in all situations Education Or Equivalent Experience A Master's degree in biostatistics, statistics or other related, scientific field and at least eight years of relevant professional experience or a combination of education and experience Benefits Why SDC SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry. We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment We strive to provide a place of belonging to our employees with fun and engaging activities from SDC's culture club We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry With a proven track record, SDC has been successfully executing client clinical programs since 2005 Take a look at how you can join our team!

Fueling Brains is a growing, vibrant organization poised to change the narrative of Education. We are looking for individuals who are passionate about transforming the world of education through a holistic, whole-brain approach to the development of young children. Children impacted by our program will grow into well-rounded, well-regulated, and joyful adults who serve their community and shape the future. We bring together the best of educational science, technology, and childcare expertise to unveil the child's infinite potential. We are looking for a Senior Neuropsychology Research Associate with a solid background in Clinical Psychology or Neuroscience to drive our research and development initiatives. This role will support product innovation, research-led strategy enhancement, and AI-powered automation of developmental data. The ideal candidate should bring in-depth knowledge of research methodologies, modern interventions, and biostatistics, with at least one research publication being a strong advantage. Key Responsibilities: Lead the audit and analysis of classroom data related to brain-based activities and outcomes. Partner with academic coaches and stakeholders to interpret child development progress and implement neuroscience-driven strategies. Oversee the mapping of developmental strategies to learning activities. Collaborate with the Application Development Team for enhancements to neuroscience-based products. Conduct literature reviews and produce research-backed recommendations for curriculum and program development. Prepare Brain Map reports and assist in data consolidation for AI model training. Supervise and review periodic activity audits to ensure alignment with neuroscience frameworks. Qualifications & Skills: Master’s degree in Clinical Psychology or Neuroscience (mandatory). 1–2 years of experience in a research or applied psychology environment. Strong proficiency in research methodology and basic biostatistics. Excellent communication and scientific writing skills. Demonstrated ability to interpret and apply scientific data in practical settings. Proficient with both conventional and modern computing systems. Experience or familiarity with AI applications in education or healthcare is a plus. Preferred: At least one research publication in a relevant field. Knowledge of modern neuroscience interventions used in child development. Experience in cognitive or behavioral developmental frameworks. Work Environment Requirements: Full-time, on-site role based in Chennai, India. Must be able to collaborate with interdisciplinary teams including Product, Data Science, and Curriculum Design. Willingness to operate in a fast-paced and research-intensive environment.

Job title: Field Bioinformatics Scientist Location: Bengaluru, Chennai or Mumbai, India Employment type: Full Time Expand Your Horizons and Promote Advanced Life Science Tools for Future Healthcare with MGI #OMICS FOR ALL #Leading Life Science Innovation About BGI BGI Group was founded in 1999 in China with the vision of using genomics for the benefit of mankind and has since become the largest genomics organization in the world. With over 10,000 employees, BGI operates in more than 100 countries, focusing on research and applications in healthcare, agriculture, conservation, and environmental fields. BGI has a proven track record of innovative, high-profile research, which has generated over 3,800 publications, with 430+ publications in top-tier journals such as Nature, Science and Cell. Additionally, in the field of R&D, BGI was ranked No.1 among corporations in the life science/biotechnology sector in the Asia-Pacific region and No.5 worldwide by Nature Index. About MGI MGI is one of the subsidiaries of BGI Group, it is committed to building core tools and technology to lead life science through intelligent innovation. With a focus on R&D, production, and sales of DNA sequencing instruments, reagents, and related products, MGI provides real-time, panoramic, and full-life-cycle equipment and systems for precision medicine, precision agriculture, precision healthcare, and other relevant industries. MGI is a leading producer and one of the few companies in the world that can independently develop and mass-produce clinical high-throughput gene sequencers, its multi-omics platforms include genetic sequencing, medical imaging, and laboratory automation. Our Mission is to develop and promote advanced life science tools for future healthcare, and to transform people’s lives for the better. We don’t hesitate to make bold decisions that can help us achieve new breakthroughs. We believe that the success of our business will mean a better world for people to live in. Our Message to the world is simple: lead in life science innovation, make everyone’s life healthier and longer. Your duties as an FBS include but are not limited to the following: Design, develop, optimize, and maintain in-house bioinformatics pipelines and various genomics applications. Understand customer research questions and provide appropriate solutions or customized approaches. Respond to technical issues from global sales and customers, providing resolutions and recommendations. Liaise with FAS, FSE, Product Managers, and R&D to provide product feedback, develop customised solutions, and support solution provision. Maintain current knowledge in Sequencing, Bioinformatics, MGI products, and industry trends Evaluate new software/tool suitability for various applications, and apply best-practice statistical and computational methods. Provide technical (FPGA) pre-sales and post-sales support services. Provide training and webinars to customers and the front-end sales team. Assist with document management, including collecting and updating training materials, FAQs, slides, videos, SOPs, and knowledge base content. The successful candidates for this position can demonstrate: Bachelor's degree or above with 3+ years’ experience in academic or industrial settings in Bioinformatics, Computational Biology, Biostatistics or Computer Science, or equivalent experience. Experience in developing next-generation sequencing data analysis methods for DNA,RNA and Long read analysis. Experience with scripting languages, including Python, bash, Perl, C++ and R. Excellent communication skills and ability to describe complex process and result to audiences with diverse backgrounds. Ability to contribute independently and collaboratively, manage progress of assigned tasks, and work in a fast-paced environment. Experience with using version control systems such as Git. Knowledge and experience with a wide range of bioinformatics tools. Proficiency in using Linux operating system such as Ubuntu, Fedora, Centos, etc. Here at BGI, we value people and consider our employees as partners. We have created a transparent, fair, and friendly environment. We implement an agile approach to management, providing each partner with enough independence as well as guidance. We take care of our partners’ physical and mental health and are dedicated to a life-work balance corporate culture. Not only do we bring life science closer to people, but we also participate in various charity programs, advocate for nature preservation, and support equality. We condemn any form of discrimination and are committed to providing job opportunities to everyone regardless of sex, race, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and more. Let’s move to a brighter and more equal future together and deliver #Omicsforall

Overview Cactus Life Sciences is a remote-first organization, and we embrace an accelerate from anywhere culture. You may be required to travel to our Mumbai office based on business requirements or for company/team events. If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Senior Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Responsibilities Taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client and audience needs with excellent attention to detail. Actively involve in reviewing materials developed by scientific writers to ensure strategic alignment and scientific accuracy as needed and providing clear constructive feedback, support, and supervision to writers. Mentor and train scientific writers by sharing best practices and client preferences, thereby contributing to skill development within the team. Having excellent knowledge of product/account to enable meaningful interactions with clients and authors, including consultancy where necessary. Building and maintaining strong, long-term relationships with international pharmaceutical clients, healthcare professionals, and key stakeholders, including authors, reviewers, and KOLs across therapeutic areas. This involves anticipating client needs, advising on strategic and tactical plans, and recommending improvements to scientific content and new ways to disseminate data effectively. Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives. Attending client and other external meetings and supporting senior team members as needed. Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. Also, supporting with the development of visual content and materials using effective data visualization techniques and approaches. Contributing to innovative “out of the box” solutions for medical writing projects. You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date. Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines. Supporting with pitches, both during the preparation phase and the actual pitch. Qualifications And Prerequisites 3-5 year of experience in relevant fields of scientific writing. PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD OR MPharm/M.Sc with a good understanding of clinical research and medical communication. Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills. Ability to adapt writing style to different materials and target audiences. Basic knowledge of biostatistics. Literature reviewing and evaluation capabilities. Very good working knowledge of MS Office. Application Process Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds. For this role, the process starts with a Technical Interview with the Hiring Managers, followed by a Technical Assessment, where candidates will have agreed upon timeline to complete the task. The final round will be the HR Interview. All interactions will be conducted virtually via MS Teams. Equal Opportunity Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from Anywhere As a remote-first organization, these are essential attributes we look for in all our candidates. Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently. Documenting work that brings everyone on the same page. Maturity to choose between synchronous and asynchronous collaboration. Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status. About CACTUS At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do. Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Job Description Position: Medical Coder - Work from Home Ct: HR KAMATCHI - 8925264660 Job Description:Medical Coding is the process of conversion of text information related to healthcare services into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books. Requirement knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills No of vacancy: 500 Eligibility Nursing GNM/DGNM Life science graduates Pharmacy Physician assistant Bio medical Engineers Bio chemistry Bio technology Bio informatics Micro biology Zoology and Advanced zoology Biology Botany Plant biotechnology Genetics Food and Nutrition Paramedical Physiotherapy M.Sc. Clinical Nutrition M.Sc. Human Genetics M.Sc. Medical Laboratory Technology M.Sc. Medical Sociology M.Sc. Epidemiology M.Sc. Molecular Virology M.Sc. Biostatistics M.Sc. Blood Banking Technology M.Sc. Rgnerative Medicine M.Optom. M.Sc. Genetic Counseling M.Sc. Radiolog Imaging Technology M.Sc. Medical Biochemistry M.Sc, Medical Microbiology M.Sc. Clinical Care Technology M.Sc. Clinical Care Technology M.Sc. Medical Physics B.Sc. - Accident Emergency Care Technology B.Sc. - Audiology speech Language Pathology B.Sc. - Cardiac Technology B.Sc. - Cardio Pulmonary Perfusion Care Technology B.Sc. - Critical Care Technology B.Sc. - Dialysis Technology B.Sc. - Neuro Electrophysiology B.Sc. - M.L.T. B.Sc. - Medical Sociology B.Sc. - Nuclear Medicine Technology B.Sc. - Operation Theatre Anaesthesia Technology Bachelor of Science in Optometry B.Sc. - Physician Assistant B.Sc. - Radiology Imaging Technology B.Sc. - Radiotherapy Technology B.Sc. - Medical Record Science B.Sc. - Respiratory Therapy B.Sc. - Fitness and Lifestyle Modifications Accident Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre Anaesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Salary 15K to 17K (fresher) To 50K (experienced) Pm (Incentives Benefits as per Corporate Standards) 4K fixed hike after six months Other Benefit Pick Up Drop Facility Food Facility Day Shift Weekend Off Reach Us HR KAMATCHI 8925264660 Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology GNM DGNM Physician assistant Anesthesia technician Perfusion Technology Medical coder Freshers Medical coding Freshers jobs in chennai Medical coding openings in chennai Wanted Medical coder Freshers jobs Medical coding Medical coder Medical coding Freshers Jobs in chennai Jobs for Passed outs Freshers jobs in chennai Jobs for freshers Nursing jobs for freshers Pharma jobs for Freshers Biotechology Jobs Microbiology jobs Biomedical jobs Bioinformatics jobs Bsc/Msc Jobs Biochemistry jobs Life science jobs in chennai Paramedical jobs in chennai Jobs in Tamilnadu Jobs in Pharmacy Jobs in Hospital Perks and Benefits Incentives Benefits as per Corporate Standards This job is provided by Shine.com

As a Geospatial Statistician and Analyst at our company, you will play a crucial role in supporting various geospatial activities and initiatives. Your expertise and skills will contribute to addressing geographic disparities in heart disease and stroke morbidity, mortality, risk factors, and prevention efforts. To excel in this role, you must hold a minimum of a Master's Degree in Statistics, Biostatistics, Epidemiology, Sociology, or Applied Mathematics. Pursuing or possessing a PhD in any of these fields would be advantageous. Your responsibilities will include analyzing spatial and spatio-temporal data, managing large datasets, and utilizing statistical software such as SAS, R, or GeoDa. Your daily tasks will involve providing administrative support for staff meetings related to Geospatial activities. This includes coordinating meeting logistics, preparing agendas, and documenting meeting minutes. Additionally, you will use Geographic Information Systems (GIS) to create maps showcasing geographic variations in heart disease and stroke indicators, cost data, and healthcare access. Furthermore, you will offer technical guidance on GIS and cartography to health department staff involved in the GIS Capacity Building Project. You will also contribute to the production of reports, presentations, and the Interactive Atlas of Heart Disease and Stroke, highlighting key findings and prevention strategies. Join our team and be part of a dynamic work environment that values integrity, commitment, and excellence. Together, we will continue to grow and make a difference in the field of geospatial analysis and public health. If you are passionate about utilizing statistics and GIS to address critical health challenges, we invite you to apply for this exciting opportunity.,

Job title : Biostatistician Technical Expert - Clinical Statistics Location : Hyderabad About The Job Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Biostatistician Technical Expert - Clinical Statistics within our Clinical Statistics Team at Hyderabad, you’ll lead/oversee statistical support of a team of senior and principal biostatisticians, be accountable for statistical aspects and deliverables of the team for several early/late phase studies. Provide directions and guidance in carrying out project assignments, interacting with other internal functions and applying advanced statistical methods while ensuring scientific integrity to project work. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Main Responsibilities Support the clinical development plan (CDP), clinical study design (including protocol development and review), the study setup and conduct. Conduct / Oversee the execution of the statistical analyses according to the SAP and ISAP, prepare statistical methods & provide statistical insight into interpretation and discussion of results sections for the clinical study report (CSR) and/or publications to ensure the statistical integrity of the content according to internal standards and regulatory guidelines and in compliance with SOPs. Serve as a biostatistical consultant for other members of the department and staff members from other statistics department within the organization. Provide mentoring and coaching advanced statistical methodologies to junior statisticians in Hub. Maintain knowledge and awareness of development in biostatistics and clinical trial methodology and regulatory requirements that impact on analysis. Accountable for all assigned statistical deliverables related to multiple studies or specific domains: statistical sections in protocol including sample size calculation, randomization specifications, and statistical methodology, Estimands etc., SAP, data surveillance, statistical analysis results for CSR and its appendices (TLGs and in-text tables). Propose, prepare and perform exploratory data analyses, ad-hoc analyses as relevant for the study or project objectives. Contribute to define and review the specific deliverables related to Transparency and Disclosure. Coordinate with study programmer the production and Qc of statistical analyses. Contribute to operation process optimization and provide inputs to statistics and quality standards. Represent statistics team to participate in scientific or technology working groups or cross function initiatives. About You Experience: 7+ years (MS) or 5+ years (PhD) of solid pharmaceutical industry experiences. Experience of project management and development preferred. Soft and technical skills: Broad knowledge and good understanding of advanced statistical concepts and techniques Demonstrated strong project/study management, interpersonal and communication skills. Good knowledge of pharmaceutical clinical development, together with early, late phase and post-marketing experiences Extensive ability to apply advanced statistical analyses using SAS and R languages. Knowledge or experience with Artificial intelligence or Generative AI is a plus Education: MS or PhD degree in Statistics or relevant fields Languages: Highly effective communication in English, both oral and written. Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. Build, develop and manage a statistics team support multiple TAs and different clinical phases Develop a career of being an influential statistician Gain international clinical trial experiences and communicate with Health Authorities worldwide “Shape the future of healthcare, empower clinical advancements as a visionary leader in a leading multinational pharmaceutical company” null Pursue Progress . Discover Extraordinary . Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

JOB SPECIFICATIONS: Bachelor's or Masters degree in relevant discipline. Minimum of 3 years’ experience in this position. Patience, understanding, and willingness to help. Proficient in Microsoft Applications, Good technical skills. Should be good in Communication, Email and Telephone etiquette. JOB DESCRIPTION: To collect, interpret and analyse the data related to hospital from all the department. To compile and analyse the data related to DNB courses conducted in the hospital. To coordinate with all departments staffs and validating the data concerning to the DNB courses To calculate sample size requirements for clinical studies. To provide statistical expertise and contributions for analyzing the data of research projects conducted by DNB pursuing doctors. To provide statistical support for the projects/studies/audits conducted by the doctors. To actively participate in scientific research committee in reviewing of research protocols and providing statistical input To provide statistical support and analyze data related to the audits conducted by the departments in the hospitals. To monitor and validate the data and providing statistical input into other discipline activities and participate in interdepartmental processes. To conduct biostatistics classes for the M.Sc. students studying in allied health science To invigilate examinations conducted by the university. To assess the performance of the students with periodic test and educational activities. To engage the students in curricular activities. Actively participate in Staff training activities. To contribute to professional conferences and Seminars in your field of expertise. To support the MRD department in collection and maintaining the data from all the departments Any other jobs assigned by the management in maintaining and improving the quality of the data. Should report to the Advisor, the Principal, and the Head of the Department.

Job Title: Senior Clinical Data Scientist / Clinical Data Analyst Experience: 7+ Years Location: Bangalore / Chennai / Hyderabad / Noida / Gurgaon (India) Industry: Pharmaceutical / Healthcare / Life Sciences Employment Type: Full-time Job Summary: We are seeking a highly experienced and analytical Senior Clinical Data Scientist / Analyst with 7+ years of experience in clinical data analysis, pharmaceutical research, and data science methodologies . The ideal candidate will have hands-on experience working with EMR/EHR data , advanced SQL , and machine learning models to derive actionable insights that support clinical research and drug development. Key Responsibilities: Analyze and interpret complex clinical and EMR data to support real-world evidence (RWE), HEOR, and clinical trial analysis. Design and develop statistical and machine learning models to predict patient outcomes, drug efficacy, and safety. Perform deep-dive analytics using Advanced SQL (CTE, RANK, PARTITION) for cohort identification and data transformation. Collaborate with cross-functional teams including biostatisticians, clinical operations, and regulatory affairs. Ensure data quality and integrity from diverse sources like EMR, claims, lab systems, and clinical trial management systems (CTMS). Automate data pipelines and implement best practices in reproducible analytics. Create dashboards, data visualizations, and reports for stakeholders and medical affairs teams. Stay up to date with current industry trends in real-world data (RWD), clinical informatics, and regulatory requirements. Required Skills: 7+ years of experience in clinical data analytics or data science within the Pharma/Healthcare domain . Strong expertise in Advanced SQL : CTEs, Window Functions (RANK, DENSE_RANK, PARTITION BY), joins, subqueries. Experience working with EMR/EHR systems such as Epic, Cerner, Meditech, etc. Proficiency in Python, R , or SAS for statistical and machine learning modeling. Strong knowledge of clinical trial design , ICD/CPT coding , MedDRA , and pharmacovigilance datasets. Hands-on with machine learning frameworks (Scikit-learn, XGBoost, etc.) for prediction and classification tasks. Familiarity with regulatory guidelines such as HIPAA , GCP , and 21 CFR Part 11 . Experience with data visualization tools such as Tableau, Power BI, or Python-based dashboards . Preferred Qualifications: Master’s or Ph.D. in Data Science, Biostatistics, Bioinformatics, Public Health, or a related field . Prior experience in RWE/RWD analytics , HEOR studies , or pharma R&D analytics . Knowledge of CDISC SDTM/ADaM standards . Experience working with cloud platforms (AWS, Azure, GCP) and data lake architecture is a plus. Job Type: Contractual / Temporary Contract length: 12 months Schedule: US shift Application Question(s): What would your NP? Which location would you pick Bangalore / Chennai / Hyderabad / Noida / Gurgaon (India) Experience: Data science: 5 years (Preferred) Machine learning: 5 years (Preferred) EMR systems: 5 years (Preferred) Work Location: In person

Job title : Biostatistician Technical Expert - Clinical Statistics Location : Hyderabad About the job Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As a Biostatistician Technical Expert - Clinical Statistics within our Clinical Statistics Team at Hyderabad, you’ll lead/oversee statistical support of a team of senior and principal biostatisticians, be accountable for statistical aspects and deliverables of the team for several early/late phase studies. Provide directions and guidance in carrying out project assignments, interacting with other internal functions and applying advanced statistical methods while ensuring scientific integrity to project work. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Main responsibilities: Support the clinical development plan (CDP), clinical study design (including protocol development and review), the study setup and conduct. Conduct / Oversee the execution of the statistical analyses according to the SAP and ISAP, prepare statistical methods & provide statistical insight into interpretation and discussion of results sections for the clinical study report (CSR) and/or publications to ensure the statistical integrity of the content according to internal standards and regulatory guidelines and in compliance with SOPs. Serve as a biostatistical consultant for other members of the department and staff members from other statistics department within the organization. Provide mentoring and coaching advanced statistical methodologies to junior statisticians in Hub. Maintain knowledge and awareness of development in biostatistics and clinical trial methodology and regulatory requirements that impact on analysis. Accountable for all assigned statistical deliverables related to multiple studies or specific domains: statistical sections in protocol including sample size calculation, randomization specifications, and statistical methodology, Estimands etc., SAP, data surveillance, statistical analysis results for CSR and its appendices (TLGs and in-text tables). Propose, prepare and perform exploratory data analyses, ad-hoc analyses as relevant for the study or project objectives. Contribute to define and review the specific deliverables related to Transparency and Disclosure. Coordinate with study programmer the production and Qc of statistical analyses. Contribute to operation process optimization and provide inputs to statistics and quality standards. Represent statistics team to participate in scientific or technology working groups or cross function initiatives. About you Experience : 7+ years (MS) or 5+ years (PhD) of solid pharmaceutical industry experiences. Experience of project management and development preferred. Soft and technical skills : Broad knowledge and good understanding of advanced statistical concepts and techniques Demonstrated strong project/study management, interpersonal and communication skills. Good knowledge of pharmaceutical clinical development, together with early, late phase and post-marketing experiences Extensive ability to apply advanced statistical analyses using SAS and R languages. Knowledge or experience with Artificial intelligence or Generative AI is a plus Education : MS or PhD degree in Statistics or relevant fields Languages : Highly effective communication in English, both oral and written. Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave. Build, develop and manage a statistics team support multiple TAs and different clinical phases Develop a career of being an influential statistician Gain international clinical trial experiences and communicate with Health Authorities worldwide “Shape the future of healthcare, empower clinical advancements as a visionary leader in a leading multinational pharmaceutical company”

As an ideal candidate for this position, you should hold a Master's degree in Pharmacy with a specialization in Pharmacology or Pharmaceutical Analysis coupled with 5-8 years of experience. Alternatively, a Ph.D. with 2-5 years of relevant experience in PK/PD Modelling and PBPK models would also be considered. Your responsibilities in this role would include developing and applying pharmacometric models to aid in drug development and regulatory submissions. You must possess a deep understanding of non-linear mixed effects modelling and be proficient in using software tools such as PBPK models, Phoenix, R, PoPK, QSP modelling, or similar platforms. Your expertise in pharmacokinetics/pharmacodynamics (PK/PD) modelling and First-in-human dose predictions will be crucial for the success of this role. Collaboration is key in this position, as you will work closely with clinical pharmacology, biostatistics, and other interdisciplinary teams to shape clinical trial designs and analyze data. Your tasks will also involve creating and executing model-based strategies to enhance dosing regimens and achieve optimal therapeutic outcomes. Ensuring the accuracy and quality of pharmacometric analyses and reports will be a significant part of your role. You will be expected to engage with regulatory agencies, preparing submission documents related to pharmacometric analyses. Staying updated on the latest advancements in pharmacometrics and integrating new methodologies and technologies as needed will be essential. Additionally, presenting your findings and strategies to project team meetings and cross-functional teams is crucial, highlighting your ability to collaborate effectively in a team environment.,

Job Overview Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports. Accountable for controlling costs and maximizing revenue recognition. Provide training, guidance and mentorship to lower level and new staff. Essential Functions Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Conducts all appropriate validation requirements, according to Standard Operating Procedures (SOPs), for each task undertaken. Checks programming logs for cleanliness and correct processing of data. Inputs into Data Issues log and follows issues to appropriate resolution. Leadership: Perform statistical team lead role on single studies. Through this, works closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget. Build and maintain effective customer relationships, driving statistical discussions, providing support and/or guidance for statistical activities. Demonstrates and promotes efficient communication. If in lead role, runs meetings, documenting where necessary and following up on actions. Actively participates in internal project team meetings, provides timely progress updates. As a lead, will have input on estimate at completion (EAC) reporting. Data Management: Assist in reviewing or advising data management staff on database design, validation checks and critical data. Handles data issue resolutions. If in lead biostatistical role, handles lock and unblinding process with appropriate supervision. Statistical Analysis Plan (SAP) and Shells: Authors or performs quality control review (QC) of SAPs and shells. Make best use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods). May author or QC complex SAPs, under supervision if needed. Datasets: Writes and maintains programming specifications. Programs assigned datasets to industry standards. Handles dataset derivations and assignment. Tables, Listings and Figures (TLFs): Writes programming specifications for statistical analyses outputs. Programs TLFs, maximizes programming efficiency with use of tools, where applicable. Checks resulting output for format and content, and questions specification as needed. Ensures consistency across items produced. Timelines: Plans and documents timelines, forecasts resource needs, suggests work may be out of scope. Financials: Shares accountability (with resource managers) for the financial success of assigned studies. Accountable for controlling costs and maximizing revenue recognition. Responsible for sharing budget expectations with the team. Raises concerns to manager if new work or rework appears to be out of scope. Understands 'scope of work' and has an awareness of contract and budget assumptions. Knowledge Sharing: Helps train staff regarding operational items. Mentors junior staff. Supports colleagues and provides motivation as needed. Risk Management: Identifies risks to project delivery and/or quality and spends time to proactively avoid as well as proposes solutions to mitigate risks. Where possible, anticipate risks to minimize need for study level escalations. Other Clinical Data Interchange Standards Consortium (CDISC) requirements: Leadership: Under supervision within Compound. May perform statistical team lead role on studies within a compound. In addition to the leadership responsibilities above, also prioritizes and takes proactive approach to gain efficiencies in work across protocols. Study Start up: Assist with protocol development, sample size calculation, protocol and case report form (CRF) review. Protocol: Authors or performs quality control (QC) review of the statistical section of a protocol (making best possible use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods). Proposals: May be able to review and comment on proposals/budgets at a study level. May contribute to request for proposals (RFP). May be expected to present at bid defenses. Clinical Study Report (CSR): Reviews or drafts CSR or statistical report. Customer: On occasion, may serve as primary point of contact for customer. May also consult on operational topics with clients. Lock and Unblinding Process: Handles the database lock and unblinding process. May participate on the biostatistics randomization team (drafts randomization specifications and/or reduce or perform quality control (QC) review of randomization schedules). May serve as unblinded lead statistician. Other Responsibilities: As defined on ad-hoc basis by managers. May assist with cross functional collaboration. Qualifications Bachelor's Degree Biostatistics or related field and 3 - 5 years relevant experience Req Or Master's Degree Biostatistics or related field and 3-5 years relevant experience Req Or Ph.D. Biostatistics or related field and 6 year relevant experience Req Typically requires 7 years of prior relevant experience, or equivalent combination of education, training and experience. Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience. Excellent written and oral communication skills including grammatical/technical writing skills. Excellent attention and accuracy with details. In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Familiarity with moderately complex statistical methods that apply to applicable clinical trials. Strong individual initiative. Strong organizing skills. Strong working knowledge of SAS computing package. Familiarity with other relevant statistical computing packages such as nQuery. Strong commitment to quality. Ability to effectively manage multiple tasks and projects. Ability to lead and co-ordinate small teams. Ability to solve moderately complex problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Working knowledge of relevant Data Standards (such as Clinical Data Interchange Standards Consortium CDISC/ADaM). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Job Title: Biostatistician under the NIHR, Global Health Surgery Research unit on Global Surgery Type of Employment : Full-time, Onsite Experience : Minimum 1 Year Location : Christian Medical College & Hospital Ludhiana Qualification : Masters or PhD in Biostatics or allied subjects Job Description: Proficiency in statistical software programs, including SPSS and R, or equivalent. Extensive experience in summarizing and presenting findings in reports. ” Good Knowledge of Biostatistical techniques in clinical trials. ” Author statistical analysis plans. '" Develop internal capacity in biostatistics via short courses and seminars Independently manage all statistical aspects of a project. Excellent knowledge of statistical principles for analysis. Managing large data sets. Good communication skills. Desirable: Experience with SAS and STATA. Experience with SPSS, R and NVIVO Application Guidelines: Qualified and Interested applicants are required to send electronic application letters with their current CVs describing their experience , qualification and two reference contacts by email. Email should be sent to globalsurgindia@cmcludhiana.in , dhruvghosh73@gmail.com, hr.office@cmcludhiana.in. Applicants should indicate in the email subject Biostatistician Position. Only shortlisted Applicants will be contacted. Job Types: Full-time, Fresher Pay: ₹60,000.00 per month Work Location: In person