- 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
- College/University degree in Life Sciences or an equivalent combination of education, training and experience
- At least 18 months prior clinical study and site startup experience
- Well-developed communication and organizational skills
- Ability to negotiate and build relationships at all levels
- Leadership, mentoring, and organizational skills
- Excellent working conditions
- Extensive training and friendly, collegial team
- Competitive salary package
- Opportunities for personal and professional growth
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Study Startup Associate - Shanghai, 中国 - PSI
描述
Job Description
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 based in Shanghai
You will:
Qualifications
Additional Information
Advance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects.
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