Leading the local study teams (consisting of monitors and study administrators) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines
Ensuring that study sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived
Ensuring timely submissions of proper application/documents to Ethic Committee/Regulatory Authority
Close communication with global study teams and overall responsibility for study commitments
Ensuring compliance of the clinical research process with ICH-GCP practices, the study protocol, AZ Global and Local Clinical SOP’s and the Ministry of Health Clinical Research Regulations

University degree, preferably from Healthcare related areas (Pharmacy, Veterinary, Chemistry, Biology, Medical etc.)
Advanced level of English
Minimum 5 year experiences in Clinical Research (preferably 2 years in Project Management positions and Biopharma specific)
Project management skills
Strong communication and negotiation skills
Ability to prioritize and handle multiple tasks
Basic coaching skills and good at team work
Financial management skills
Effective planning and organizational skills with result-oriented approach
Stakeholder management experience
Analytical thinking, critical reasoning ability
Good command of MS Office applications
No restriction to travel
Driving License
No military obligation for male candidates

Local Study Associate Director – Biopharma

Key skills