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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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Real-World Data Analyst

Bristol Myers Squibb

2-3 years

August 4, 2025

Online Application

Safety Scientist

ICON plc

3 Years+

August 4, 2025

Online Application

Safety Aggregate Report Coordinator

IQVIA

Freshers

August 3, 2025

Email Application

Production / QC / QA / Engineering & Maintenance

Cohance Lifesciences

2 - 14 years

August 1, 2025

Walk In Interview

Medical Surveillance Specialist 1

IQVIA

2-6 years

July 31, 2025

Online Application

Apprenticeship Program

Eurofins Advinus

Freshers

July 26, 2025

Walk In Interview

Regulatory Affairs Specialist

IQVIA

5+ years

July 25, 2025

Email Application

Pharmacovigilance Quality Assurance Specialist

Wipro

3-6 Years

July 25, 2025

Email Application

Production / R&D / Warehouse / Engineering & Maintenance

Cohance Lifesciences

2-6 years

July 25, 2025

Walk In Interview

Health Economics Consultant (Modelling)

Parexel

3+ years

July 24, 2025

Online Application

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