Take your career to the next level and lead challenging study activation process on a country/regional level. You will support clinical research teams and ensure PSI projects start smoothly and on time.
Office Base: Shanghai China
You will:
- Maintains study-specific and corporate startup tracking systems.
- Facilitates site budgets and contract negotiations.
- Supports site regulatory document collection.
- Under supervision may prepare initial submission dossiers to competent authorities ethics committees and/or site submission dossiers (as applicable).
- Communicates with the project team and investigational sites throughout the study startup phase.
- Develops site specific startup timelines and enrollment projections and is responsible for meeting the site activation milestones.
- May review study specific translations.
- Supervises Trial Master File (TMF) maintenance throughout the study startup phase.
Qualifications :
- Bachelors degree of Medical Pharmaceutical or any Life Sciences related major
- At least 4 years site startup experience
- Well-developed communication and organizational skills
- Ability to negotiate and build relationships at all levels
- Leadership mentoring and organizational skills
- English and Japanese skills (High Business level to Fluent)
Additional Information :
Advance your career in clinical research coordinating a variety of tasks and learning new things while growing with a rapid growing company that puts its people first!
Remote Work :
No
Employment Type :
Full-time