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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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Graduate Pharmacovigilance Associate

ICON

0 - 1 Years

August 17, 2026

Online Application

Drug Safety Associate

Novotech

2–4 Years

August 17, 2026

Online Application

Pharmacovigilance Scientist

Safetypulse247

0 - 3 Years

August 16, 2026

Online Application

Centralized Monitoring Assistant

IQVIA

6 Months - 2 Years | Freshers can Apply Too

August 15, 2026

Online Application

Statistical Programmer – Clinical SAS

Indero

1 year

August 14, 2026

Online Application

Trainee Statistical Programming

Caidya

0 - 1 Years

August 14, 2026

Online Application

TMF Specialist I

ICON

Prior clinical research or document management experience preferred

August 14, 2026

Online Application

Quality Specialist

PrimeVigilance

Prior experience in a Quality and/or Compliance role.

August 13, 2026

Online Application

Medical Writer I

ICON

2+ years of related experience

August 13, 2026

Online Application

SPE Pharmacovigilance

Cognizant

2–4 years

August 13, 2026

Online Application

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