Clinical Program Manager (m/f/d)
If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the live of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.
What the job looks like
Each day you´ll enjoy a variety of challenges, such as:
- Provide strategic operational input into Clinical Development Plan (CDP) with respect to operational aspects and requirements, including definition of timelines/milestones and resource needs
- Steer and oversee the planning, set-up, conduct and closure of the assigned projects and inherent clinical trials, including trial budgets, rolling forecasts and timelines/milestones
- Oversee adherence to Clinical Trial Protocols and applicable guidelines, laws and regulations as well as the contractual agreements with the assigned Vendors
- Analyze and evaluate the impact of anticipated, new and updated project risks for the clinical trials
- Review and assess performance (quality, timelines, budget) of Vendors and proactively initiate mitigations and improvements
What you´ll bring to the table
To make the most of this role and truly thrive, you should have:
- 10+ years related experience in a pharmaceutical company, biotech firm, or CRO, which should include at least 8 years of operational and managerial experience in planning/start-up and execution of clinical trials
- MsC, preferably in life or natural sciences; PMP certification is a plus
- Specific CRO experience is a plus
- International and intercultural working experience in Clinical Development
- Proven ability to work independently and to lead multidisciplinary trial teams in a complex matrix environment
- Proven experience in developing effective relationship with Vendors (including budget negotiations and contracting)
- In depth knowledge of Clinical Development from phase I to phase III