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- Tasks: Lead international clinical studies and manage project delivery from start to finish.
- Company: Join a dynamic CRO focused on innovative clinical research.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on process improvement and career development.
- Why this job: Make a real impact in oncology and rare diseases while managing exciting projects.
- Qualifications: Experience in clinical project management and multi-country studies is essential.
The predicted salary is between 50000 - 70000 £ per year.
Location: France, Spain or United Kingdom
Working model: Remote / home-based
Sector: CRO / Clinical Research
Therapy area focus: Oncology, rare disease and complex clinical studies
Are you an experienced Clinical Project Manager looking for a role where you can take genuine ownership of international clinical studies while remaining close to the operational delivery of the trial? We are supporting a confidential CRO client with the appointment of a Clinical Project Manager to join their European project management team. This is an opportunity to play a key role in the delivery of complex clinical studies across multiple countries, working closely with sponsors, CRAs, sites, vendors and cross-functional internal teams.
This role would suit someone who enjoys balancing strategic project oversight with hands-on clinical operations involvement. You will be comfortable managing timelines, budgets, risks, vendors and client communication, while also staying close to site performance, recruitment, monitoring quality and study delivery.
The role
As Clinical Project Manager, you will be responsible for the planning, coordination and delivery of assigned clinical studies from site selection through to close-out. You will act as a key point of contact for the sponsor and will lead the internal project team to ensure studies are delivered to agreed scope, timelines, quality expectations and budget.
Responsibilities will include:
- Leading the delivery of international clinical studies across multiple countries
- Acting as the primary contact between the CRO and sponsor
- Managing project plans, timelines, trackers, study documentation and operational delivery
- Leading cross-functional project teams across clinical operations, regulatory, medical, biometrics, pharmacovigilance and vendor functions
- Overseeing study start-up, site selection, site activation, recruitment, monitoring quality and close-out activity
- Working closely with CRAs and site teams to ensure strong clinical delivery and issue resolution
- Managing project risks and developing mitigation plans
- Overseeing vendors including laboratories, drug distributors, IRT providers and other study partners
- Managing budgets, revenue forecasting, scope changes and change order requirements
- Providing regular written and verbal updates to sponsors and internal stakeholders
- Ensuring studies are delivered in line with ICH GCP, local regulations, SOPs and project agreements
- Supporting audit and inspection readiness at project, country and site level
- Contributing to process improvement initiatives within the project management group
About you
We are looking for someone with strong clinical research project management experience, ideally gained within a CRO environment. You may currently be working as a Clinical Project Manager, Project Manager, Senior Clinical Trial Manager, Global Trial Manager or similar. What matters most is that you have personally managed multi-country clinical studies and can demonstrate both project leadership and hands-on operational oversight.
You will ideally bring:
- Clinical research experience within a CRO, pharmaceutical or biotech environment
- Previous project management experience across clinical trials
- Experience managing multi-country or international studies
- A strong understanding of ICH GCP, clinical trial operations and regulatory requirements
- Experience working closely with CRAs, investigational sites and cross-functional study teams
- Confidence managing timelines, risks, vendors, budgets and sponsor communication
- Experience in oncology, rare disease, CNS, cell and gene therapy, autoimmune or other complex therapeutic areas would be advantageous
- The ability to work independently in a leaner, collaborative CRO environment
- Residence in France, Spain or the United Kingdom
Clinical Project Manager employer: Quiddity Talent Solutions
Contact Detail:
Quiddity Talent Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Project Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work in CROs. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by practising common questions related to project management and clinical trials. We recommend role-playing with a friend or using online resources to get comfortable discussing your experience in managing multi-country studies.
✨Tip Number 3
Showcase your hands-on experience! During interviews, highlight specific examples of how you've managed timelines, budgets, and vendor relationships in previous roles. This will demonstrate your ability to balance strategic oversight with operational delivery.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Clinical Project Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Project Manager role. Highlight your experience in managing multi-country clinical studies and any specific therapeutic areas you've worked in, like oncology or rare diseases. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your skills make you the perfect fit for this role. Don't forget to mention your hands-on experience with project management and operational delivery.
Showcase Your Achievements: When detailing your experience, focus on your achievements rather than just responsibilities. Use metrics where possible to demonstrate your impact, like successful study deliveries or budget management. We love seeing how you've made a difference in previous roles!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re proactive and keen to join our team!
How to prepare for a job interview at Quiddity Talent Solutions
✨Know Your Clinical Research Inside Out
Make sure you brush up on your clinical research knowledge, especially in oncology and rare diseases. Be prepared to discuss specific studies you've managed, focusing on your role in project oversight and operational delivery.
✨Showcase Your Project Management Skills
Highlight your experience with managing timelines, budgets, and risks during the interview. Use concrete examples from past projects to demonstrate how you successfully navigated challenges and ensured study delivery.
✨Familiarise Yourself with ICH GCP and Regulations
Since compliance is key in clinical trials, be ready to talk about your understanding of ICH GCP and local regulations. This will show that you’re not just a manager but also someone who prioritises quality and adherence to standards.
✨Prepare for Cross-Functional Collaboration Questions
Expect questions about how you work with CRAs, vendors, and internal teams. Prepare examples that illustrate your ability to lead cross-functional teams and resolve issues effectively, showcasing your collaborative spirit.