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...