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Clinical Project Manager/Senior Project Manager - Renal; Europe
Remote / Online - Candidates ideally in
3000, Bern, Canton de Berne, Switzerland
Listed on 2026-06-30
3000, Bern, Canton de Berne, Switzerland
Listing for:
Emerald Clinical
Remote/Work from Home
position Listed on 2026-06-30
Job specializations:
-
Management
Program / Project Manager, Operations Manager
Job Description & How to Apply Below
About The Role
We are seeking an experienced Project Manager to join our growing team in Europe. This is a home‑based role providing flexibility while allowing the candidate to lead global and regional clinical trials across multiple therapeutic areas. The ideal candidate has experience managing Renal clinical trials and a strong background in project leadership, financial oversight, and strategic trial execution.
Responsibilities- Provide strong, independent leadership for assigned clinical projects, ensuring successful execution.
- Serve as the primary point of contact for clients, vendors, and internal stakeholders.
- Oversee study management activities, including site selection, initiation, monitoring, and closeout.
- Develop and maintain study timelines, budgets, and project plans, ensuring adherence to scope.
- Mitigate risks and proactively address challenges to keep projects on track.
- Ensure compliance with ICH‑GCP, regulatory guidelines, and company SOPs.
- Manage vendor relationships and study‑specific contracts.
- Provide mentorship and guidance to junior project team members.
- Support proposal development, bid defense meetings, and business growth initiatives.
- Participate in internal and external project team meetings to ensure alignment and success.
- Bachelor’s or Master’s degree in a science or related field.
- Previous experience working on clinical projects within an academic, CRO, or pharmaceutical company environment.
- Experience in Renal clinical trials is mandatory.
- Approximately seven (7) years of industry experience. A minimum of two (2) years of Project Management experience within the CRO industry is mandatory; prior experience as a CRA, in site management, trial coordination, or other relevant industry experience is preferred.
- Experience managing single or multiple regions, working across different therapeutic indications, managing full‑service studies, and working across early phase to late phases of clinical trials.
- Excellent working knowledge of, and ability to implement project activities in accordance with, ICH/GCP and all applicable regulations and guidelines in the relevant regions.
- Previous exposure to client‑facing interactions and/or client management.
- Project finance management experience, preferentially within a CRO.
- Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
- Flexibility:
Hybrid or remote working arrangements, depending on your location and role. - Career Growth:
Access to a wealth of learning opportunities and a global network of scientific leaders. - Employee Wellbeing:
Programs and initiatives designed to promote work‑life balance, health, and team connection, including global engagement surveys, recognition programs, and team‑building events. - Global Opportunities:
Exposure to diverse projects and clients across an international reach.
We are an equal‑opportunity employer and encourage applications from all qualified candidates.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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