HGRAC specialist
ICON · Beijing, China
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Role summary
ICON seeks a Senior Study Start Up Associate for its Beijing office to lead site activation and initiation activities in a sponsor-dedicated model. The role involves feasibility assessments, regulatory submissions, and informed consent document development within a fast-paced clinical research environment.
What they're looking for
- Bachelor's degree or equivalent in medical or scientific discipline
- Minimum 3 years of clinical study start-up and site activation experience
- Fluency in local Chinese language and English
- Ability to work independently and mentor others
- Willingness to travel approximately 5% as required
- Legal right to work in China
What you'll be doing
- Lead site feasibility assessments, identification, and contract negotiations
- Provide technical expertise to study start-up team leads and project teams
- Prepare and coordinate regulatory and ethics submissions for compliance
- Develop and review informed consent forms and subject information sheets
Privacy & handoff
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