Offer summary
Qualifications:
Substantial experience in rare diseases or genetic medicines, Expertise in clinical development programs, Proven track record managing clinical studies, Experience with CROs and vendors, Ability to manage and mentor reports.
Key responsabilities:
- Manage high-level aspects of clinical studies
- Oversee internal Clinical Operations team
- Ensure execution of study plans and timelines
- Develop recruitment strategies for clinical trial enrollment
- Prepare for regulatory filings and communication