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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

Science & Medical Affairs

Bioinformatics Biostatistics Data Science & Analytics Clinical SAS Programming HEOR & Real-World Evidence Medical Writing Scientific Writing Medical Science Liaison

Manufacturing & Quality

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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November 1, 2026

November 1, 2026

Safety & PV Specialist I Literature Case Processing

Syneos Health

2+ Years

October 31, 2026

Online Application

Data Entry Operator

Wembrace Biopharma

0–1 Years

October 31, 2026

Online Application

Statistical Programmer

Emmes CRO

0 - 3 Years

October 30, 2026

Online Application

Medical Science Liaison – Immunology

Johnson & Johnson

0 - 3 Years

October 30, 2026

Online Application

CDM Programmer II

Thermo Fisher

2+ years of CDM experience and Medidata Rave or Veeva CDB expertise

October 30, 2026

Online Application

October 30, 2026

Central Monitor, Data Surveillance, Clinical Data Sciences

Pfizer

1 Years+

October 29, 2026

Online Application

Analyst

IQVIA

Freshers

October 28, 2026

Online Application

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