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Responsibilities:
- Independently oversee all aspects of study site management, including patient safety, data quality, and audit readiness.
- Manage site start-up procedures, regulatory submissions, and investigator contract negotiations.
- Conduct all types of site visits and prepare accurate monitoring reports.
Minimum Requirements:
- 4-year college degree in a scientific or healthcare discipline.
- 5+ years as a CRA in CRO or pharma/biotech industry.
- English proficiency at professional level.
Preferred Qualifications:
- Graduate or postgraduate degree in a relevant field.
- Experience in rare and complex therapeutic areas.
- Ability to travel up to 60% on average.
Precision Medicine Group
Precision Medicine Group is a global precision medicine company that supports clinical research and development. The company fosters a collaborative culture with a focus on quality and professional growth.