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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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Officer – Regulatory Affairs

Lambda CRO

1–4 Years

March 3, 2026

Online Application

Executive/Sr Executive – Medical Affairs

Hetero

1–4 years

March 3, 2026

Online Application

Healthcare Data Analyst

Global Value Web

Freshers

March 3, 2026

Online Application

Sr Drug Safety Associate

Clinexel

3+ years

March 3, 2026

Email Application

Product Support Specialist I

Advarra

1 - 3 Years

March 2, 2026

Online Application

Pharmacovigilance Representative

2Coms (Accenture)

Freshers

March 2, 2026

Email Application

Bioanalytical Experts – LCMS/MS & BA/BE

BioRadius

1.5 – 10 years

February 28, 2026

Email Application

FSP Medical Writer & Document Review Specialist

Thermo Fisher Scientific

2+ years

February 27, 2026

Online Application

GMP QA roles, Clinical Research Associate jobs, Pharmacovigilance aggregate report jobs, or engineering

Pharmazone

1 - 10 Years`

February 27, 2026

Online Application

CDM Programmer, Safety Writers, PV Manager & Business Analyst

Thermo Fisher Scientific

3 - 8 Years+

February 26, 2026

Online Application

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