Job Description
Overview
As Study Manager you will lead and coordinate the delivery of clinical and evidence generation studies from planning through close‑out. You will work with study teams, vendors, and country colleagues to keep studies on time, on budget, and compliant with standards. We value clear communication, practical problem solving, and a focus on quality.
Responsibilities
- Monitor study conduct and progress; identify, resolve and expedite risks and issues.
- Draft and review key clinical documents (Protocol, ICF) and study plans.
- Coordinate meetings and collaboration with internal teams and external partners (CROs, vendors).
- Support GSM in CRO oversight and delivery of delegated activities.
- Serve as primary vendor contact for study‑specific deliverables.
- Provide country‑level oversight: recruitment, data completeness, deviations, regulatory compliance.
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