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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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Regulatory Affairs Officer II

IQVIA

5–6 years

August 4, 2026

Online Application

Scientific Affairs Intern

Indus Biotech

Freshers

25,000 per month

August 4, 2026

Email Application

ICSR Case Processing Associate (SPE) / Quality Review Associate (SME)

2coms

1–5 Years

August 4, 2026

Online Application

Central Monitor II

Precision Medicine

Minimum 2 Years

August 4, 2026

Online Application

RA GRSSC Intern – Regulatory Affairs Internship

Novartis

Freshers

August 4, 2026

Online Application

Medical Writer II (MLR Reviewer)

Syneos Health

Experience with Medical Writing and MLR Review.

August 4, 2026

Online Application

Sr CD Project Support Assistant

IQVIA

1 year of relevant experience in clinical research or project support.

August 3, 2026

Online Application

Medical Science Liaason – Immunology

Johnson & Johnson Innovative Medicine

0–3 Years

August 3, 2026

Online Application

Associate Medical Writer

Thermo Fisher

1–3 years of relevant experience.

August 3, 2026

Online Application

Programmer & CRA Roles

Fortrea

2 - 5 Years

August 3, 2026

Online Application

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