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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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Young Professional Program

Reliance Life Sciences

Freshers

3.2 – 4.5 LPA

September 18, 2025

Walk In Interview

Drug Safety Associate

Indegene

September 18, 2025

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Clinical Research Associate (CRA II/Sr CRA I), Clinical Trial Manager II, Site Contract Specialist, and Sr Clinical Operations Specialist

Syneos Health

2–5+ years

September 17, 2025

Online Application

CDM Programmer II (SAS)

Thermo Fisher Scientific

5+ years

September 17, 2025

Online Application

Medical Surveillance Specialist

IQVIA

2–6 years

September 16, 2025

Online Application

Pharmacovigilance Associate

Accenture

0 - 3 Years

3- 4 LPA

September 16, 2025

Online Application

Safety Science Coordinator I

Fortrea

0 - 1 Years

September 15, 2025

Online Application

Intern – Scientific Affairs Team, Clinical Trial Assistant, Senior Pharmacovigilance Reporting Associate, Lead Clinical Data Science Programmer

ICON plc

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Stats

September 15, 2025

Online Application

Life Science Recruiter (US Staffing)

Unicon Pharma

0-1 Year

September 13, 2025

Walk In Interview

Real World Data Analyst I & Data Scientist I

Bristol Myers Squibb

0 - 3 Years

September 12, 2025

Online Application

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