Clinical Project Manager
vor 4 Monaten
For our client, a well-known pharmaceutical company in Basel, we are looking for a Clinical Project Manager (M/F/d).
**Background**
The Study Leader/Clinical Scientist will manage and support global clinical trials, focusing primarily on low-complexity studies while providing expertise for high-complexity trials. This role involves leading protocol development, executing study plans, and collaborating with cross-functional teams to ensure successful trial outcomes. The position requires effective risk management, budget oversight, and data interpretation to drive clinical and regulatory success.
**General Information**:
- Start date: ASAP
- Duration: 18 months
- Extension: Possible
- Workload: 100%
- Work location: Basel
**Tasks & Responsibilities**:
- Lead the creation and management of clinical protocols and related documents, collaborating with medical leads and cross-functional teams to ensure accurate and comprehensive study documentation
- Develop and implement study-level operational plans, working with key partners to ensure strategic alignment, effective execution, and adherence to study goals and timelines
- Identify and select high-performing study sites, working closely with cross-functional teams to meet recruitment targets and ensure sites are equipped to meet study requirements
- Conduct ongoing review and interpretation of clinical trial data, including safety trends and study results, collaborating with medical experts to generate actionable insights and reports
- Forecast and manage study budgets, implement risk mitigation strategies, and ensure efficient resource allocation to minimize variance and address potential challenges in trial execution**Must Haves**:
- Advanced degree in life science/healthcare or equivalent education/degree in life sciences/ healthcare
- 2+ years’ experience in clinical trials/development
- Proficiency in English (written and spoken)
- Strong understanding of clinical trial methodology with a focus on early development, and experience in managing multiple trials
- Familiarity with ICH-GCP guidelines, external regulations, and internal policies, ensuring adherence to quality standards and effective management of clinical trial processes
- Expertise in operational project management, planning, prioritization, and problem-solving, along with knowledge of clinical finance principles to manage budgets and minimize variance
**Contact**:
Jan Schmitz-Elsen
Team Lead Talent Acquisition
+41 79 425 10 45
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