Beschreibung
Clinical Research Study Leader - Basel, Switzerland - 6 Month Contract
Background:
The role of the Clinical Research Study Leader is to provide leadership for one or more global Study Management Teams responsible for delivering internally managed as well as outsourced First in Man through Proof-of-Concept studies. The CRSL is accountable for the strategic and tactical study activities, ensuring high quality execution standards within the agreed budget and timelines.
Tasks & Responsibilities:
- Leads the cross-functional Study Management Team (SMT). In the SMT Leader (SMTL) role, the CRSL is responsible for the planning, coordination, communication, motivation and setting the direction of the SMT, including obtaining agreement on study required timelines, budgets, objectives and goal setting. The SMTL is accountable for the delivery of the clinical studies within the agreed timelines, budget, and quality.
- Prepares and manages the budget/financial plan including overall study and site-level costs, collaborating with the respective stakeholders in contract negotiations and preparation, payment schedule and tracking.
Must haves:
- Minimum 5 years in study management with extensive experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies management, sample management, conduct and monitoring of clinical studies.
- Minimum Bachelor (preference on Master) in Life Sciences
- Experience with global study management.
- Experience in pharma (preferred) or CRO.
- Experience with early phases of clinical trials
- NS & Infection & Oncology