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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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Associate Proposal Developer

IQVIA

0 - 1 Years

August 25, 2026

Online Application

eClinical Coordinator

Medpace

0 - 2 Years (Intern Experience Preffered)

August 24, 2026

Online Application

Analyst Clinical Data Management

Syngene

Experienced Candidates

August 24, 2026

Online Application

Clinical Project Coordinator Entry

Medpace

1 - 3 Years | Freshers can Apply Too

August 24, 2026

Online Application

Regulatory Affairs – DCGI

Raptim Research

1–4 Years

August 21, 2026

Online Application

Clinical Data Analyst II

Parexel

4 Years+

August 21, 2026

Online Application

Medical Writers

Insignia Clinical Services

1 Years+

August 21, 2026

Email Application

Clinical Trial Finance Associate and Clinical Trial e-Source Designer

KCRS

Freshers

August 21, 2026

Email Application

Clinical Data Svs Associate | Clinical Data Services – Clinical EDC Build

Accenture

0–3 Years

August 20, 2026

Online Application

CDM

Clinovo

3+ years

August 20, 2026

Email Application

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