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Clinical Study Project Manager

Clinical Study Project Manager

Infotree Global SolutionsPoland
Ponad 30 dni temu
Typ pracy
  • Quick Apply
Opis pracy

At Infotree, meeting your career needs is a top priority. Client satisfaction is largely dependent on the resources we can provide, and we take pride in our delivery. We have a supportive team in place to give quality people a chance to grow and challenge themselves in their roles which has resulted in that we have placed many employees in positions that have grown into lifelong careers.

We have a team of dedicated recruiters and consultant care representatives that are committed to your success and well-being. Check out our open roles to get started.

Infotree Poland Sp. z o.o. is part of Infotree Global Solutions. Agency number : 15970.

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, fast-paced 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 cutting-edge medical research is conducted to the highest standards.

Your Role & Responsibilities :

As a Clinical Study Project Manager, you will be responsible for end-to-end 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 study-related 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 start-up to close-out .
  • 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 We’re Looking For :

We’re seeking a proactive and detail-oriented professional with a strong scientific background and proven clinical project management experience . To succeed in this role, you should have :

  • Master’s degree in a science / health-related field.
  • Project management experience in multi-center clinical studies (minimum 3 years).
  • Experience in at least one of the following areas :
  • Full-cycle project management in multi-center clinical studies (from start-up to close-out).
  • Start-up phase project management in multi-center clinical studies.
  • Working knowledge of Good Clinical Practice (GCP) .
  • Strong communication, collaboration, and leadership skills .
  • Excellent problem-solving 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 multi-center studies.

    Conducting tenders (bidder selection, negotiations, contract development).

    Hands-on experience in multi-center, multi-country 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 . You’ll 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 you're ready to take on a leadership role in clinical study management and contribute to life-changing medical advancements, apply now!

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