Clinical Trial Manager

Lead global innovation in renal care by steering high‑impact clinical trials from concept to completion.

R&D Partners is seeking a Clinical Trial Manager to lead the design, planning, execution, and oversight of global clinical studies for the Renal Denervation portfolio. This role involves managing cross-functional clinical teams to support product development and commercialization objectives. The ideal candidate will bring deep expertise in clinical trial operations, a strong understanding of regulatory requirements, and technical knowledge specific to the therapeutic area.

This is a fully remote role based anywhere in Europe.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Lead the development of clinical strategy and trial design by collaborating with relevant departments and stakeholders.
• Write study protocols, protocol amendments, informed consents, project plans, and timelines.
• Manage clinical study timelines and budgets, including vendor selection and contract management.
• Oversee the development of internal and external project materials, processes, manuals, and regulatory submissions.
• Ensure continuous audit readiness of the study team.
• Proactively identify, assess, and manage clinical study risks and emerging trends.
• Facilitate communication between internal teams, investigators, and investigational sites through meetings, updates, and correspondence.
• Interact with regulatory agencies and facilitate regulatory submissions in collaboration with Regulatory Affairs.
• Present scientific data at industry gatherings, investigational meetings, and regulatory agency meetings.
• Provide accurate progress reports on clinical projects for submission to regulatory agencies and ethics committees.

Key Skills and Requirements:

Required Qualifications:

• Minimum 5 years of related work experience with a Bachelor’s degree or 3 years with a Master’s degree.
• Proven clinical trial experience (Sponsor or CRO).
• Advanced knowledge of Good Clinical Practices (GCP), ISO 14155, and FDA regulations governing clinical trials.
• Experience working with external vendors and Contract Research Organizations (CROs)
• Fluency in French is a necessity for this role.

Preferred Qualifications:

• Experience with medical device clinical trials.
• Experience in cardiovascular therapeutic areas.
• Proven ability to navigate cross-functional group dependencies and relationships.

For more information, please contact Antonia Ray.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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