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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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Product Support Specialist

Advarra

1-3 years

August 6, 2025

Online Application

Due Diligence Specialist

ICON

1-4 years

August 6, 2025

Online Application

Medical Device Consultant

IQVIA

4 - 6 Years

August 6, 2025

Online Application

Pharmacovigilance QA

Pharmazone

6-10 yrs

August 6, 2025

Email Application

Safety & PV Specialist

Syneos Health

1 - 3 Years

August 5, 2025

Online Application

Business Development Executive

SpinoS Life Science

Freshers

August 5, 2025

Email Application

Database Management Specialist - SAS Programmer

IQVIA

1 - 2 Years

August 5, 2025

Online Application

Safety Aggregate Report Specialist 2

IQVIA

3-4 years

August 5, 2025

Online Application

Safety Aggregate Report Specialist

IQVIA

1 - 3 Years

August 5, 2025

Online Application

Project Support Coordinator in Clinical Research

Thermo Fisher Scientific

0 - 4 Years

4 - 5 LPA

August 4, 2025

Online Application

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