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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 & Safety

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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Data Acquisition Associate

Clario

1 year

August 31, 2026

Online Application

Supplier Qualification Associate

Fortrea

1–3 Years

August 31, 2026

Online Application

PV Officer – Medical Device & Product Experience

PrimeVigilance

1 - 4 Years+

August 31, 2026

Online Application

Data Analyst & Medical Writer Jobs

IQVIA

0 - 3 Years

August 31, 2026

Online Application

Data Analytics Consultant

IQVIA

2 - 4 Years

August 31, 2026

Online Application

Lab Data Analyst

IQVIA

2–3 years of Clinical Data Management and SAS Programming experience.

August 31, 2026

Online Application

Drug Safety Specialist I / II

Syneos Health

1–6 Years

August 31, 2026

Online Application

Pharmacovigilance Associate

iCRO

Freshers

August 30, 2026

Online Application

Safety Aggregate Report Specialist

IQVIA

1–2 years

August 28, 2026

Online Application

Medical Writer Jobs – CSR Narratives

Syneos Health

1 - 2 Years

August 27, 2026

Online Application

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