Local Study Associate Director - Sponsor Dedicated (m/w/d)
IQVIA UK
United Kingdom
Lead local study team at country level
Ensure ich-gcp and local regulation compliance
Manage site identification and qualification process
The role requires leading Local Study Teams to deliver clinical studies according to agreed resources, budgets, and timelines while ensuring strict compliance with international guidelines
Job Summary
The role requires leading Local Study Teams to deliver clinical studies according to agreed resources, budgets, and timelines while ensuring strict compliance with international guidelines.
Responsibilities include overseeing the entire site lifecycle from identification and qualification through initiation, monitoring, and closure, as well as managing country-level financial agreements.
Candidates must possess strong leadership skills to optimize team performance, proactively identify risks, and coordinate effectively with global stakeholders and regulatory authorities.
Matching Summary
The role requires leading Local Study Teams to deliver clinical studies according to agreed resources, budgets, and timelines while ensuring strict compliance with international guidelines.
Skills & Requirements
Must-have
Lead Local Study Team at country level
Ensure ICH-GCP and local regulation compliance
Manage site identification and qualification process
Oversee study budget and financial agreements
Coordinate regulatory submissions to EC/IRB
Nice-to-have
Proven ability to motivate cross functional teams
Excellent negotiation and interpersonal skills
Experience with risk management plans
Ability to adapt to IT systems quickly
Strong project management capabilities
Key Requirements
Bachelor degree in life science or related discipline
Minimum 3 years experience in Development Operations (CRA/SrCRA)
Good knowledge of ICH GCP and local regulations
Excellent English and local language proficiency
Willingness to travel nationally and internationally