Job Description
Job Summary
Manage the design and launch of clinical research studies, owning start‑up deliverables and ensuring quality execution across sponsors, CROs, and internal teams.
Responsibilities
- Develop and manage study database design requirements for protocols, amendments, and sponsor changes.
- Configure and oversee study databases in alignment with clinical protocols and sponsor standards.
- Act as the primary set‑up point of contact for sponsors and internal stakeholders.
- Coordinate start‑up activities across Data Management, Logistics, Clinical Trial Materials, Laboratory Testing, and Specimen Management.
- Maintain and communicate project timelines, action logs, issue logs, and status reports during start‑up.
- Proactively manage scope changes, identify risks, and implement contingency plans.
Qualifications
- Bachelor’s degree in science or a related field.
- Exper...