The Global Study Associate Manager provides oversight to ensure efficient study delivery in partnership with clinical experts and external service providers
Job Summary
The Global Study Associate Manager provides oversight to ensure efficient study delivery in partnership with clinical experts and external service providers.
This role requires maintaining interactions with internal functions like Data Management and Regulatory while managing relationships with CROs to meet time, cost, and quality objectives.
Candidates must adhere to global clinical processes and international guidelines such as ICH/GCP to ensure the study remains inspection ready at all times.
Matching Summary
The Global Study Associate Manager provides oversight to ensure efficient study delivery in partnership with clinical experts and external service providers.
Skills & Requirements
Must-have
3+ years pharmaceutical industry experience
Knowledge of ICH/GCP guidelines
Clinical development process expertise
CRO management and oversight skills
Trial Master File quality verification
Nice-to-have
Experience with non-drug project work
Strong leadership and independent work abilities
Advanced computer proficiency
Basic knowledge of GMP/GLP outside GCP
Key Requirements
University degree in medical or biological sciences
At least 3 years of relevant industry experience
Excellent verbal and written English communication skills