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Clinical Research Clinical Data Management (CDM)Pharmacovigilance Medical Writing Trial Master File (TMF)Medical Coding SAS Data Sciences Medical Science Liaison (MSL)Medical Reviewer RWE / HEOR

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Clinical Research Clinical Data Management Pharmacovigilance Trial Master File (TMF)Regulatory Affairs Medical Reviewer Medical Coding Pharmacist Medical Devices

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Bioinformatics Biostatistics Data Science & Analytics Clinical SAS Programming HEOR & Real-World Evidence Medical Writing Scientific Writing Medical Science Liaison

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Quality Assurance (QA)Quality Control (QC)Pharmaceutical Production R&D & Formulation Pharmaceutical Microbiology Pharmaceutical Packaging Pharmaceutical Warehouse Pharmaceutical Engineering Environmental Health & Safety Effluent Treatment Plant (ETP)Technology Transfer (TDS)

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Junior & Regulatory Affairs Associates

Parexel

0 - 4 Years

April 29, 2026

Online Application

Decision Analytics Associate Consultant

ZS

April 28, 2026

Online Application

TMF Specialist I

Syneos Health

1 Years+

April 28, 2026

Online Application

Sample Information Coordinator II

Labcorp

April 28, 2026

Online Application

Pharmacovigilance Trainee Junior Data Analyst

Cognizant

Freshers

April 27, 2026

Email Application

IRT Coordinator (CDM)

alimentiv

1–3 years experience in clinical trials, IRT, or data management

April 27, 2026

Online Application

Statistical Programmer – RBQM R Programming

Fortrea

3 years of experience in R programming

April 27, 2026

Online Application

Medical Report Reviewer

VitalityBSS

Freshers

April 27, 2026

Online Application

Data Review Specialist (Stability Protocol / Study Build Review)

Eurofins

4–6 years

April 27, 2026

Online Application

Associate – GRAAS Operations (GSIM Regulatory Data Management)

Amgen

April 27, 2026

Online Application

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