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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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Database Associate II (CDM)

Fortrea

1 Years+

February 26, 2026

Online Application

Drug Safety Associate

Syneos Health

2.5–4.5 years

February 25, 2026

Online Application

Regulatory Affairs Associate

Parexel

2 - 6 years

February 25, 2026

Online Application

Global Trial Associate

Bristol Myers Squibb

2 - 4 Years

February 25, 2026

Online Application

Patient Safety Specialist

Parexel

2 Years+

February 25, 2026

Online Application

Scientist Medical Writing

ClinChoice

3 years

February 24, 2026

Online Application

Pricing and Proposals Specialist

Clario

2+ years

February 24, 2026

Online Application

eCRF / Database Developer

Eurofins India Biopharma Services

2–5 years

February 24, 2026

Online Application

Operations Coordinator 1

IQVIA

Freshers

February 24, 2026

Online Application

Analytical Monitors | RBM

Johnson & Johnson

4 - 6 Years+

February 24, 2026

Online Application

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