Last updated: 2025-05-22

34 Clinical Data And Biostatistics jobs in Bengaluru.

Hiring now: Experienced I Statistical @ Johnson Jo, Sr Clinical Data Associat @ Precision , Sr External Data Spec @ Eclinical , Statistical Programmerii @ Parexel, Sr Analyst Ii Clinical Da @ Precisionm, Biostatistician @ Alimentiv, Scientific Data Analyst @ Pfm, Sr Analyst Biostatisticia @ Stryker, Statistical Programmer Ii @ Alexion, Regional Medical Advisor @ Dr Reddys .Explore more at at kaamvaam.com

🔥 Skills

Clinical Trials (7) clinical trials (6) data management (5) clinical trial (5) clinical data (4) data analysis (4) SQL (4) regulatory submissions (4) Biostatistics (3) quality control (3)

📍 Locations

Bengaluru (34)

Johnson & Johnson

Skills & Focus: Statistical Programming, Clinical Research, Data Analysis, Quality Control, Regulatory Compliance, Biostatistics, Data Structures, SAS, R, Python
About the Company: A healthcare company focused on innovative medicine and MedTech solutions.

Precision Medicine Group

Skills & Focus: data management, clinical trial, quality control, data entry, database development, clinical databases, medical coding, project management, SOPs, data review
Experience: 5+ years’ experience

Eclinical Solutions

Skills & Focus: external data management, clinical data, local lab data, data transfer agreements, data quality, ICH/CGP compliance, data validation, vendor data processing, data transfer, data integrity
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 5+ years

Johnson & Johnson

Skills & Focus: Regulatory Affairs, Data Management, MDRiM, Data Quality, Compliance, MedTech, Medical Device, Process Improvement, Database Management, Cross-functional Environment
About the Company: Johnson & Johnson is a global healthcare company that focuses on innovative medicine and medical technology, creating solutions for complex diseases.
Experience: 3+ years
Type: Hybrid

Parexel

Skills & Focus: statistical programming, clinical trials, biostatistics, data management, sponsor teams, therapeutic areas, functional service provider, programming languages, data analysis, clinical research

Johnson & Johnson

Skills & Focus: Clinical Data Management, Pharmaceutical, Data Analytics, Clinical Trials, Regulatory Guidelines, Data Review, CRO, Clinical Data Standards, Data Privacy, Cross Functional Stakeholders
About the Company: A multinational healthcare company focused on pharmaceuticals, medical devices, and consumer health products.
Experience: 5+ years in pharmaceutical, CRO or biotech industry
Type: Hybrid

Precisionmedicinegroup

Skills & Focus: Tableau dashboards, SQL programming, clinical data management, discrepancy management, data analysis, data visualization, protocol information, quality assurance, data validation, clinical trials

Alimentiv

Skills & Focus: biostatistics, clinical trials, data management, statistical planning, design, analysis, reporting, project life cycle, subject matter expert, quality auditing
About the Company: A global research organization focused on supporting clinical trials and data management.

Pfm

Skills & Focus: Data Analysis, SQL, Tableau, Data Visualization, Clinical Data, Healthcare, Data Management, Data Integrity, Regulatory Standards, Data Interpretation
Experience: 3+ years in a similar role, preferably in clinical or healthcare setting

Eclinical Solutions

Skills & Focus: Clinical Data Management, data cleaning, database design, protocol conversion, data review, analytics, cloud SaaS, EDC systems, project management, regulatory compliance
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 5+ years in Clinical Data Management preferred

Stryker

Skills & Focus: SAS, programming, clinical trial, statistical analysis, data manipulation, quality control, data listings, report generation, EDC systems, biostatistics
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology, and Orthopaedics that help improve patient and healthcare outcomes. Alongside its …
Experience: 5-8 years
Type: Full Time
Benefits: Health benefits include medical and prescription drug insurance, dental insurance, vision insurance, critical illness i…

Eclinical Solutions

Skills & Focus: Clinical Data Management, Database Design, Data Cleaning, Quality Control, Data Verification, Project Management, Client Relationship Management, ICH/GCP Guidelines, EDC Systems, Data Reporting Tools
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 8-10 years of experience in Clinical Data Management

Pfm

Skills & Focus: regulatory documents, FDA, EMA, regulatory submissions, document management, eCTD, clinical trial applications, regulatory guidelines, submission processes, system functionality
Experience: 3 years in document management

Eclinical Solutions

Skills & Focus: SAS programming, clinical trials, data extraction, TLG programming, SDTM, ADaM, NDA filings, ICH/GCP guidelines, clinical trial methodologies, data presentations
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 7+ years in Pharmaceutical/Biotechnology industry or equivalent IT consulting role preferred.

Precision Medicine Group

Skills & Focus: clinical monitoring, report review, SOP, protocols, projct management, quality improvement, clinical trials, risk assessment, mentoring, regulatory compliance
Experience: Minimum 3 years experience in clinical monitoring, clinical trial management or equivalent

Alexion

Skills & Focus: statistical programming, SAS Programming, CDISC standards, datasets, tables, listings, figures, Good Clinical Practices, regulatory requirements, drug development
About the Company: At AstraZeneca, we champion diversity in a patient-driven, energizing, and kind culture where people build connections to explore new ideas that profoundly imp…
Experience: 2 to 4 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.

Precision Medicine Group

Skills & Focus: data management, clinical trials, database development, quality control, clinical data, data entry, SOPs, medical coding, EDC, stakeholders
About the Company: Precision Medicine Group provides data management support and assistance in all aspects of the clinical trial data management process.
Experience: 5+ years of experience

Pfm

Skills & Focus: Tableau, SQL, clinical trial, data management, dashboard, discrepancy management, data quality, data visualization, clinical data, database management

Precision Medicine Group

Skills & Focus: Clinical Systems Administration, eTMF, CTMS, IRT, EDC, User Access Management, Data Entry, Help Desk Support, Clinical Trials, System Modifications
Experience: 2 years of clinical trial experience with 2 years of experience with Clinical Systems

Parexel

Skills & Focus: Project Leadership, Clinical Trials, Project Plans, Clinical Research, Biostatistics, Statistical Programming, Compliance, SOPs, ICH, GCP
About the Company: Parexel is a leading global biopharmaceutical services organization that helps clients accelerate the development of innovative therapies and provide market ac…

Dr. Reddy's Laboratories Ltd.

Skills & Focus: medical affairs, thought leaders, treatment trends, medical education, strategic medical affairs plan, scientific data, patient outcomes, disease trend analysis, pharmaceutical, clinical research
About the Company: Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations.
Experience: Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs
Benefits: personalised learning programs, joining & relocation support, family support (Maternity & Paternity benefits), learning…

Precisionmedicinegroup

Skills & Focus: regulatory documents, FDA, EMA, clinical trial, eCTD, submission, regulatory compliance, document management, regulatory guidance, clinical research
Experience: 3 years in document management
Type: Full-time

Astrazeneca

Skills & Focus: Regulatory Information Management, pharmaceutical, regulatory data standards, data analysis, stakeholder management, regulatory submissions, collaboration, compliance, global regulatory operations, life sciences
About the Company: AstraZeneca is a global biopharmaceutical company that focuses on innovative medicines to address unmet medical needs.
Experience: University degree in the life sciences or equivalent experience in pharmaceutical/medical industry.
Type: Full time

Johnson & Johnson

Skills & Focus: Clinical Programming, Data Analytics, Biostatistics, Data Manipulation, Clinical Safety Review, Visualization, Reporting Solutions, Stakeholder Management, Project Management, CDISC
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 4+ years of relevant experience in pharmaceutical industry is desired.
Type: Hybrid

Precisionmedicinegroup

Skills & Focus: regulatory submissions, regulatory documentation, compliance, FDA, EMA, clinical trial, document management, regulatory guidelines, eCTD, submission processes
Experience: 1-2 years

Reveal Healthtech

Skills & Focus: Life Sciences, Solution Architecture, Drug Development, Cloud Platforms, AI/ML, Healthcare, Clinical Trials, Pharmaceutical Research, Compliance, Technical Guidance
About the Company: Reveal HealthTech is a dedicated healthcare-focused technology services company – helping our clients with a range of AI and product engineering services. Reve…
Experience: 5+ years of experience in solution architecture or technical leadership roles within life sciences or health tech industries.
Benefits: Industry-best compensation and benefits.

Novo Nordisk

Skills & Focus: Clinical Trials, CVD, CKD, NASH, Research, Medical Guidance, Training, Communication, Stakeholder Engagement, Healthcare Research
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases, focusing on diabetes and expan…
Experience: 2+ years of clinical or pharmaceutical industry experience

Saama Technologies Inc

Data Manager Bengaluru
Skills & Focus: Data Management, Clinical Trials, Machine Learning, Artificial Intelligence, EDC, IRT systems, Data Quality Checks, CDISC Standards, SQL, Customer Success
Experience: 10-15 years industry experience

Iqvia

Skills & Focus: study design, edit specifications, quality delivery, eCRF, EDC build components, Study Authorization Form, Internal Design Review Meeting, database design, LLRR data, Rights and Roles
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Astrazeneca

Skills & Focus: statistical strategy, pharmaceutical industry, leadership, project management, CRO collaboration, clinical studies, data analysis, methodology expertise, regulatory submissions, cross-functional collaboration
About the Company: AstraZeneca is a global biopharmaceutical company that focuses on the discovery, development, and commercialization of innovative medicines.
Experience: Extensive experience working as a statistician in the pharmaceutical industry.
Type: Full time
Benefits: Flexibility to create one's schedule and time management, growth-oriented environment.

Saama Technologies Inc

Skills & Focus: Implementation, Clinical Trials, Lifesciences, SQL, APIs, Integrations, Agile, FDA regulations, Product Lifecycle, Healthcare Software
Experience: 3-5 years as a Product Manager or 1-2 years as a Product Owner

Iqvia

Skills & Focus: medical review, adverse events, pharmacovigilance, safety data, clinical data, regulatory requirements, safety profiles, signal detection, aggregate reports, GCP
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Three (3) years experience practicing clinical medicine after award of medical degree.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.