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- Tasks: Manage global clinical trials and lead project planning for new studies.
- Company: Dynamic pharmaceutical company focused on innovative clinical solutions.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by overseeing critical clinical trials.
- Qualifications: Experience in pharmaceutical clinical trials and strong project management skills.
- Other info: Join a collaborative team with a focus on continuous improvement and global impact.
The predicted salary is between 48000 - 72000 £ per year.
The Senior Clinical Project Manager (sCPM) is responsible for the end-to-end operational management and oversight of pharmaceutical clinical trials within a global program. This is a hands-on execution role that requires the ability to manage the day-to-day delivery of clinical trials while contributing to high-level lifecycle management discussions and program strategy.
The successful candidate will support an existing study team on an ongoing global program while also taking the lead on new studies. This role acts as a key link within the Clinical Operations department, ensuring seamless delivery across the clinical development lifecycle from pre-clinical stages all the way through.
Responsibilities- Lead the end-to-end operational management of pharmaceutical clinical trials, with a focus on a global multi-centre Phase IIa study in Pancreatic Insufficiency.
- Lead the planning and preparation for upcoming Phase IIb and Phase III transitions, ensuring all operational requirements are lined up for the next phases.
- Take full ownership of a confidential Phase I study within the same program, managing it from startup through to completion.
- Provide high-level oversight of the clinical development lifecycle, including participating in lifecycle management (LCM) discussions.
- Deliver hands-on project management, supporting existing Project Managers while simultaneously running independent studies.
- Oversee CROs and external vendors to ensure delivery to timelines, budget, and quality standards.
- Facilitate collaboration across global functions to drive inspection readiness and continuous improvement.
- Relevant pharmaceutical clinical trial experience (Pharma, Biotech, or CRO).
- Proven experience in Pharmaceutical studies is essential (Nutritional study experience is a plus but Pharma background is the priority).
- Extensive experience across the full trial lifecycle, specifically moving studies from Phase II into Phase III.
- Strong experience in Global Multi-centre study management.
- Proficient in ICH-GCP, CFR, and applicable regulatory guidelines.
- Work Pattern: Remote with a link to the London (Victoria) hub.
- Travel: Approximately 20% travel required, including quarterly meetings in London and travel to Switzerland as necessary.
Senior Clinical Project Manager in London employer: Randstad UK
Contact Detail:
Randstad UK Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Project Manager in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of the clinical trial lifecycle. Be ready to discuss your hands-on experience with Phase II and III studies, as well as how you've managed teams and projects in the past.
✨Tip Number 3
Showcase your leadership skills! During interviews, highlight specific examples where you've led teams or projects successfully. This will demonstrate your ability to take charge and deliver results in a fast-paced environment.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got a range of exciting roles, and applying directly can give you an edge. Plus, it shows your enthusiasm for joining our team at StudySmarter!
We think you need these skills to ace Senior Clinical Project Manager in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Project Manager role. Highlight your relevant experience in managing clinical trials, especially in global multi-centre studies. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of your project management skills and how you've successfully led clinical trials in the past. We love a good story!
Showcase Your Knowledge: In your application, don’t forget to mention your understanding of ICH-GCP, CFR, and other regulatory guidelines. We’re looking for someone who knows the ins and outs of the clinical development lifecycle, so let us know what you know!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss any important updates. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Randstad UK
✨Know Your Trials Inside Out
Make sure you’re well-versed in the specifics of clinical trials, especially those related to Phase II and III studies. Brush up on your knowledge of the lifecycle management discussions and be ready to discuss how you’ve successfully managed similar projects in the past.
✨Showcase Your Leadership Skills
As a Senior Clinical Project Manager, you’ll need to demonstrate your ability to lead teams effectively. Prepare examples of how you’ve overseen project delivery, managed CROs, and facilitated collaboration across global functions. Highlight your hands-on approach and how it has driven success in previous roles.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to managing clinical trials. Think about challenges you might face in transitioning studies from Phase II to III and how you would address them. This will show your problem-solving skills and strategic thinking.
✨Understand Regulatory Guidelines
Familiarise yourself with ICH-GCP, CFR, and other relevant regulatory guidelines. Be prepared to discuss how you ensure compliance in your projects and how you keep up-to-date with any changes in regulations. This knowledge is crucial for the role and will set you apart from other candidates.
