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 research.
- Why this job: Take ownership of impactful clinical trials in oncology and rare diseases.
- 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 Stockport 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 benefiting from 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 Stockport
✨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
Get your LinkedIn game on point! Make sure your profile highlights your experience in managing multi-country clinical studies. Engage with relevant content and connect with industry professionals to increase your visibility.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of ICH GCP and clinical trial operations. Be ready to discuss specific challenges you've faced in previous roles and how you tackled them—this shows you're hands-on and ready for the role!
✨Tip Number 4
Don't forget to apply through our website! We love seeing candidates who are genuinely interested in joining our team. Plus, it gives us a chance to see your application in the best light possible.
We think you need these skills to ace Clinical Project Manager in Stockport
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 Stuff
Make sure you brush up on your clinical research knowledge, especially around oncology and rare diseases. Familiarise yourself with ICH GCP guidelines and be ready to discuss how you've applied these in past projects.
✨Showcase Your Leadership Skills
Prepare examples that highlight your experience in leading cross-functional teams and managing multi-country studies. Be specific about the challenges you faced and how you overcame them, as this will demonstrate your project management prowess.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to risk management or vendor oversight. Think through your approach to problem-solving and be prepared to articulate your thought process clearly.
✨Communicate Effectively
Since you'll be the primary contact for sponsors, practice articulating complex information in a straightforward manner. Show that you can keep stakeholders informed and engaged throughout the study lifecycle.
