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Senior Clinical Project Manager CR&D - Opportunity for Growth and Success

Our client, one of the fastest-growing pharma companies in Switzerland, is seeking a Senior Clinical Project Manager CR&D to join their dynamic team. With massive employment growth over the past year, this is a great opportunity to be part of a company that is experiencing large growth in revenue and employment. As a serious professional looking to progress in your career, here you don't have to wait for someone to quit - you can readily step into a challenging role and make a significant impact.

- Join a company that is at the forefront of the pharmaceutical industry, driving innovation and delivering life-changing therapies to patients.
- Be part of a company that has seen rapid growth and is positioned for continued success.
- Work in a dynamic and collaborative environment where you will have the opportunity to develop your skills and expertise and make a real difference in patient care.

Responsibilities:
- Plan, implement, and evaluate global clinical Phase 1-4 GCP studies, ensuring compliance with protocols and overall clinical objectives.
- Provide input to overall clinical development programs with coagulation and critical care products, and lead the development of study protocols.
- Evaluate, analyze, and interpret clinical data, preparing study reports, CTDs, summary reports, expert statements, etc.
- Keep track of study budgets and be involved in vendor oversight.
- Interact with Independent Data Monitoring and Steering Committees, representing Clinical Research at meetings with Competent Authorities.
- Contribute to publications and prepare abstracts, posters, and presentations for national and international congresses.
- Stay up-to-date with current knowledge of all aspects of clinical studies through reviewing scientific literature and attending conferences and seminars.

Requirements:
- PhD or MD background.
- Minimum of 5 / 10 years of experience in clinical research (as CPM / 10 years for Senior CPM) in a pharmaceutical or biotechnology company.
- Keen attention to detail and ability to work within stipulated timeframes and deadlines, even with multiple responsibilities or projects.
- Engaging and convincing personality for team building and leading a team.
- Experience in writing clinical study procedures and other clinical documents.
- Preferably experienced in the field of coagulation and critical care.
- Excellent problem-solving skills with the ability to resolve trial issues on a daily basis.
- Strong project management skills and planning competencies to set plans and execute on time and within budget.
- Experience managing CROs and outside vendors to plan and execute Phase 1- 4 clinical trials.
- Excellent presentation skills and expertise in stakeholder management.
- Demonstrated ability to collaborate, multi-task, and work effectively in a fast-paced matrix environment.
- Fluent in German and English (written and spoken).
- Willingness to travel up to 30%.

Contact me for more details:

• email address: a.andreenkova@nonstop-recruitment.com

For a confidential discussion about this role, or to apply, then send your CV to a.andreenkova@nonstop-recruitment.com or call me, Angelina Andreenkova, Search Specialist - Life Sciences - Switzerland, at +41 435 080 817 (intern 3594). Please feel free to visit my Linked-in profile to see my references/recommendations.

NonStop is one of the largest and fastest-growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labour leasing licences across Switzerland.