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- Tasks: Lead and manage early-phase clinical trials, ensuring compliance and quality across multiple sites.
- Company: Join a dynamic team at a leading clinical trial provider in London.
- Benefits: Collaborative environment, professional growth opportunities, and the chance to make a real impact.
- Why this job: Be at the forefront of clinical research, driving innovation and integrity in healthcare.
- Qualifications: 5+ years in clinical project management with a life sciences degree.
- Other info: Mentorship opportunities and a chance to work with diverse teams globally.
The predicted salary is between 48000 - 72000 £ per year.
Job Description
Location: Nucleus Network – Hammersmith Medicines Research – London
Why Join Us?
You’ll be part of a dynamic team committed to advancing clinical research with integrity and innovation. We offer a collaborative environment, opportunities for professional growth, and the chance to make a meaningful impact in the field of clinical development by working with a leading, early-phase clinical trial provider.
About the Role:
We are seeking an experienced and driven Senior Clinical Project Manager to lead and oversee the planning, execution, and delivery of complex early phase clinical trials. This role is ideal for someone with a strong background in managing both Phase 1 trials involving healthy participants and multi-centre studies across diverse geographies.
Key Responsibilities:
- Lead the end-to-end management of clinical trials, ensuring compliance with regulatory requirements and internal SOPs.
- Oversee Phase 1 and 2a trials with healthy and patient participants, ensuring safety, ethical standards, and scientific integrity.
- Manage multi-centre studies, coordinating across sites to ensure consistency and quality of data.
- Lead and facilitate key meetings, including Site Initiation Visits (SIVs), progress meetings with Sponsors and vendors and safety review committee meetings ensuring clear communication, alignment of objectives, and timely resolution of any issues.
- Develop and maintain project timelines, plans, budgets, and risk mitigation strategies.
- Collaborate with cross-functional teams including clinical, medical writing, data management, and biostatistics.
- Serve as the primary point of contact for sponsors, CROs, and site investigators.
- Provide mentorship, training and guidance to junior clinical project managers.
- Oversee external vendors, ensuring deliverables meet quality standards, timelines, and contractual obligations.
Requirements:
- Life sciences degree or equivalent.
- Minimum of 5 years’ experience in clinical project management.
- Proven track record managing early-phase trials with healthy participants.
- Experience leading multi-centre patient studies, preferably in a global setting.
- Strong knowledge of ICH-GCP and UK regulatory guidelines.
- Excellent communication, leadership, and organisational skills.
- Ability to work independently and manage multiple priorities.
Desirable:
- Higher degree
- Experience with electronic trial master files
- Experience of regulatory and ethics submissions in the UK using IRAS.
- Knowledge of US regulations
Clinical Project Manager employer: Nucleus Network
Contact Detail:
Nucleus Network 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, attend industry events, and join relevant online forums. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Be ready to discuss how your experience aligns with their goals, especially in managing early-phase trials. Show them you’re not just another candidate, but someone who genuinely cares about their mission.
✨Tip Number 3
Practice your pitch! You want to be able to clearly articulate your experience and how it relates to the role of Clinical Project Manager. Keep it concise and impactful, focusing on your leadership skills and successful project outcomes.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take that extra step to connect with us directly.
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 with early-phase trials and multi-centre studies, as we want to see how your background aligns with our needs.
Craft a Compelling Cover Letter: Your cover letter should tell us why you’re passionate about clinical research and how you can contribute to our dynamic team. Share specific examples of your past successes in managing trials to grab our attention!
Showcase Your Skills: Don’t forget to highlight your knowledge of ICH-GCP and UK regulatory guidelines. We’re looking for someone who can hit the ground running, so make sure we see your relevant skills front and centre.
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 don’t miss out on any important updates from our team!
How to prepare for a job interview at Nucleus Network
✨Know Your Trials
Make sure you brush up on your knowledge of Phase 1 and 2a trials, especially those involving healthy participants. Be ready to discuss your previous experiences managing these types of studies, as well as any challenges you faced and how you overcame them.
✨Showcase Your Leadership Skills
As a Clinical Project Manager, you'll need to demonstrate strong leadership abilities. Prepare examples of how you've led teams, facilitated meetings, and resolved conflicts in past projects. Highlight your experience in mentoring junior project managers, as this will show your capability to guide others.
✨Understand Regulatory Requirements
Familiarise yourself with ICH-GCP and UK regulatory guidelines. Be prepared to discuss how you've ensured compliance in your previous roles. This will not only show your expertise but also your commitment to maintaining high standards in clinical research.
✨Communicate Clearly
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely. During the interview, make sure to listen actively and respond thoughtfully to questions, demonstrating your ability to align objectives and resolve issues promptly.