Clinical Trial Principal (Remote - US)
Remote · United States
Job Summary
Lead clinical trial activities across the study lifecycle with strategic guidance and mentorship. Develop and maintain clinical trial documentation; perform advanced clinical support including documentation for product registration and statistical analysis; coordinate regulatory submissions and ensure adherence to GCP, ISO 14155, and applicable regulations. Oversee site performance, generate clinical trial reports, prepare ethics submission materials (protocols, CRFs, patient/investigator brochures, informed consent), verify data consistency with clinical notes, and support statistical plans. Drive continuous improvement of clinical processes and collaboration with Regulatory Affairs for product registration documentation. Requires periodic travel in the United States; bachelor’s degree, GCP certification, and 7+ years of relevant experience are expected.
Required Qualifications
- Bachelor’s degree in a relevant field
- Good Clinical Practices certification
- Knowledge in Systematic literature search Zotero/Mendeley
- Medical Device Regulation
- Advanced English C1
- 7+ years of experience on similar roles
- Microsoft Office suite (Word, Excel, PowerPoint, Planner, etc.)
Desired Qualifications
- Good Clinical Practices certification
- Knowledge in Systematic literature search Zotero/Mendeley
- Medical Device Regulation
- Advanced English C1
- Microsoft Office suite (Word, Excel, PowerPoint, Planner)
- 7+ years of experience in similar roles
- Bachelor’s degree in a relevant field
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.