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 trials.
- 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
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 in Liverpool employer: Quiddity Talent Solutions
Join a dynamic and innovative CRO that prioritises employee growth and development, offering a collaborative work culture where your contributions directly impact the success of international clinical studies. With the flexibility of remote working from France, Spain, or the United Kingdom, you will enjoy a supportive environment that values strategic oversight alongside hands-on involvement in complex clinical trials, particularly in oncology and rare diseases. Our commitment to excellence ensures that you will have access to continuous learning opportunities and the chance to lead impactful projects across multiple countries.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Project Manager in Liverpool
✨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 and scenarios related to project management in clinical trials. We recommend role-playing with a friend or using online resources to boost your confidence.
✨Tip Number 3
Showcase your hands-on experience! When discussing your background, highlight specific projects where you managed timelines, budgets, and teams. 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 in Liverpool
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 knowledge of clinical research, especially in oncology and rare diseases. Familiarise yourself with ICH GCP guidelines and be ready to discuss how you've applied these in your previous roles.
✨Showcase Your Project Management Skills
Prepare specific examples that highlight your experience managing multi-country studies. Be ready to discuss how you handled timelines, budgets, and risks, and how you ensured effective communication with sponsors and cross-functional teams.
✨Demonstrate Your Hands-On Approach
This role requires a balance between strategic oversight and operational involvement. Share instances where you’ve been hands-on in site management or issue resolution, showcasing your ability to lead while staying close to the action.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to clinical trials and their expectations for the role. This shows your genuine interest and helps you assess if the company aligns with your career goals.
