Clinical Study Project Manager
Clinical Study Project Manager
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Job Description
Clinical Study Project Manager Drive Innovation in Medical Research
Are you passionate about advancing medical research and bringing innovative healthcare solutions to the world Do you thrive in a dynamic fastpaced environment where collaboration and strategic execution are key If so we have the perfect opportunity for you!
We are looking for a Clinical Study Project Manager to lead the preparation and execution of a clinical performance study and contribute to the global registration and certification of in vitro medical devices. This role offers a unique chance to work at the intersection of R&D and clinical operations ensuring that cuttingedge medical research is conducted to the highest standards.
Your Role & Responsibilities:
As a Clinical Study Project Manager you will be responsible for endtoend management of clinical studies overseeing the process from initial planning to completion. Your key duties will include:
- Selecting negotiating and contracting clinical study vendors.
- Leading tenders preparation and execution with external consulting partners.
- Developing studyrelated documents in collaboration with internal teams and contracted CROs.
- Participating in feasibility and site selection processes for clinical studies.
- Creating and overseeing the recruitment strategy ensuring studies meet required participant numbers.
- Acting as the main point of contact leading and managing studies from startup to closeout.
- Coordinating with internal and external stakeholders to ensure timely execution and budget control.
- Supporting quality assurance process implementation for clinical and medical research activities.
What Were Looking For:
Were seeking a proactive and detailoriented professional with a strong scientific background and proven clinical project management experience. To succeed in this role you should have:
Masters degree in a science/healthrelated field.
Project management experience in multicenter clinical studies (minimum 3 years).
Experience in at least one of the following areas:
- Fullcycle project management in multicenter clinical studies (from startup to closeout).
- Startup phase project management in multicenter clinical studies.
Working knowledge of Good Clinical Practice (GCP).
Strong communication collaboration and leadership skills.
Excellent problemsolving and planning abilities.
Ability to work independently and within set timelines.
Fluent English skills (verbal and written).
Proficiency in clinical study management tools and software.
Preferred (Bonus) Experience:
Candidates with additional expertise in the following areas will be given priority:
Project management of IVD studies (2 years).
Oversight of external vendors (CROs central labs etc.).
Vendor and clinical site contracting for multicenter studies.
Conducting tenders (bidder selection negotiations contract development).
Handson experience in multicenter multicountry clinical studies (CRA Data Manager Feasibility Specialist etc.).
Why Join Us
In this role you will be at the forefront of groundbreaking medical advancements working in an environment that values innovation collaboration and excellence. Youll have the opportunity to shape the future of clinical research lead impactful projects and work alongside a highly skilled and passionate team.
Flexible working environment
Engaging and impactful projects
Career growth opportunities
Work with leading experts in the field
If youre ready to take on a leadership role in clinical study management and contribute to lifechanging medical advancements apply now!
Employment Type
Full Time
