At a Glance
- Tasks: Lead international clinical studies and manage project delivery from start to finish.
- Company: Confidential CRO with a focus on innovative clinical research.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Join a dynamic team and contribute to groundbreaking clinical research.
- Why this job: Make a real impact in oncology and rare diseases while leading complex projects.
- Qualifications: Experience in clinical project management and multi-country studies required.
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 involves:
- 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 in Bournemouth employer: Quiddity Talent Solutions
Join a dynamic and innovative CRO that prioritises employee growth and development, offering a collaborative work culture where you can take ownership of international clinical studies from the comfort of your home in France, Spain, or the United Kingdom. With a focus on oncology and rare diseases, this role provides unique opportunities to engage in complex clinical trials while enjoying flexible working arrangements and a supportive team environment that values your contributions.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Manager in Bournemouth
✨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 or even referrals.
✨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 with your responses.
✨Tip Number 3
Showcase your hands-on experience! During interviews, highlight specific examples of how you've managed timelines, budgets, and teams in previous roles. This will demonstrate your ability to take ownership of complex studies.
✨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 in Bournemouth
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 through our website for the best chance of getting noticed. It’s super easy and ensures your application goes directly to us. Plus, we can’t wait to see what you bring to the table!
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. Familiarise yourself with ICH GCP guidelines and the specific regulations relevant to the countries involved in the studies you'll be managing.
✨Showcase Your Project Management Skills
Prepare to discuss your previous experiences managing multi-country clinical studies. Be ready to share specific examples of how you've handled timelines, budgets, and risks, as well as how you’ve led cross-functional teams to success.
✨Communicate Like a Pro
Since you'll be the primary contact between the CRO and sponsors, practice articulating your thoughts clearly and confidently. Think about how you can convey complex information simply and effectively during the interview.
✨Demonstrate Your Problem-Solving Abilities
Be prepared to discuss challenges you've faced in past projects and how you resolved them. Highlight your ability to develop mitigation plans and ensure smooth study delivery, as this will show your hands-on operational oversight.
