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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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Quality Control Specialist (Medical Writing)

Excelya

1 - 5 Years

January 10, 2025

Online Application

Pharmacovigilance Associate/Senior Associate Role

ICON

1 - 6 years

Not Disclosed

January 9, 2025

Online Application

Pharmacovigilance Reporting Associate

Icon Plc

1- 3 Years

4.5 - 5 Lacs per year

January 9, 2025

Online Application

Regulatory & Start-Up Specialist 1

IQVIA

1 - 2 Years

January 9, 2025

Online Application

Biostatistician

Indira IVF

1-6 years

January 9, 2025

Walk In Interview

Safety Associate Trainee

IQVIA

0 - 1 Years

January 9, 2025

Online Application

Safety Associate Trainees

IQVIA

Freshers

January 8, 2025

Email Application

Analyst

IQVIA

0 - 3 Years

January 7, 2025

Online Application

Project Specialist

Parexel

1 - 5 Years

January 6, 2025

Online Application

Medical Writer

Zoe MedCare

2 Years

January 4, 2025

Online Application

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