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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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Safety Operations Specialist I

Novo Nordisk

6 years of experience

March 5, 2025

Online Application

Centralized Monitoring Assistant

IQVIA

6 Months to 2 Years

March 5, 2025

Online Application

Senior Clinical Data Associate, Document Management Associate, and Clinical Document Specialist

Novotech

1 - 6 Years

March 5, 2025

Online Application

Principal Programmer Analyst (Pharmacovigilance)

Thermo Fisher Scientific

5 - 12 Years

March 5, 2025

Online Application

Medical Science Liaison - Cardiovascular

Bristol Myers Squibb (BMS)

1 - 2 Years

March 5, 2025

Online Application

Medical Reviewer, R Programmer, and Medical Data Reviewer

TCS

1 - 5 Years

March 4, 2025

Walk In Interview

Report Writer Coordinator I

Labcorp

1 - 3 Years

March 4, 2025

Online Application

Safety Science & Regulatory Operations roles

Fortrea

2 - 6 Years

March 4, 2025

Online Application

Clinical Research Associate

CBCC Global Research

3 - 8 Years

March 3, 2025

Email Application

Statistical Programmer II, Senior Statistical Programmer, Principal Statistical Programmer

Syneos Health

2 - 8 Years +

February 28, 2025

Online Application

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