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- Tasks: Lead complex clinical studies from start to finish, ensuring success and quality.
- Company: Join a dynamic team in a leading clinical research environment.
- Benefits: Competitive daily rate, remote work flexibility, and potential for long-term opportunities.
- Other info: Remote role with the option to work onsite in Central London.
- Why this job: Make a real impact in healthcare by managing innovative clinical trials.
- Qualifications: Proven experience in study management and strong leadership skills.
The predicted salary is between 30000 - 40000 £ per year.
Type: Temporary
Duration: 7 months approx. (until end of 2026)
Location: Remote (client based in London)
Rate: circa. £(Apply online only) per day (via Umbrella, INSIDE IR35)
We are seeking multiple experienced Study Managers to oversee the delivery of complex studies from initiation through to completion. This is a key role requiring strong leadership, operational oversight, and the ability to drive high-quality study execution in a fast-paced environment. This role is ideal for candidates with solid Study Management experience who can confidently take ownership of study delivery and drive successful outcomes.
Key Responsibilities
- Manage end-to-end study delivery, ensuring milestones, timelines, and budgets are met
- Act as the primary point of accountability for study execution and performance
- Coordinate cross-functional teams (clinical, data, regulatory, vendors) to ensure alignment
- Oversee study planning, risk management, and issue resolution
- Ensure compliance with regulatory requirements, SOPs, and quality standards
- Manage vendor relationships and external partners to ensure effective delivery
Skills & Experience Required
- Proven experience as a Study Manager (essential) with ownership of full study life-cycle
- Strong understanding of clinical/trial or research study processes and governance
- Demonstrated ability to manage multiple stakeholders and cross-functional teams
- Experience with Oncology, Respiratory and/or Cardiovascular clinical trials
- Excellent project management, planning, and organisational skills
- Strong leadership, communication, and problem-solving capabilities
- Experience working within regulated environments (e.g. GCP or equivalent) is highly desirable
NOTE: These roles are remote however, if you would be interested in working with the client longer-term, they encourage workers to be onsite 3 days per week (offices in Central London).
Global Clinical Study Manager in London employer: Carbon 60
Contact Detail:
Carbon 60 Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Clinical Study 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 a lead or can put in a good word for you.
✨Tip Number 2
Prepare for those interviews! Research the company and the specific studies they’re involved in. Tailor your answers to highlight your experience with study management and how you can drive successful outcomes.
✨Tip Number 3
Showcase your leadership skills! During interviews, share examples of how you've coordinated cross-functional teams and managed stakeholders effectively. This will demonstrate your ability to take ownership of study delivery.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities that match your skills. Plus, it’s a great way to ensure your application gets seen by the right people.
We think you need these skills to ace Global Clinical Study Manager in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Global Clinical Study Manager role. Highlight your experience in managing complex studies and any relevant skills that match the job description. We want to see how you can take ownership of study delivery!
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 leadership and project management skills, and don’t forget to mention your experience with Oncology, Respiratory, or Cardiovascular trials.
Showcase Your Teamwork Skills: Since this role involves coordinating cross-functional teams, make sure to highlight your ability to work collaboratively. We love seeing candidates who can manage multiple stakeholders and keep everyone aligned towards common goals.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get you one step closer to joining our team!
How to prepare for a job interview at Carbon 60
✨Know Your Studies Inside Out
Before the interview, make sure you’re well-versed in the specifics of clinical study management. Brush up on your experience with Oncology, Respiratory, and Cardiovascular trials, as these are key areas for the role. Be ready to discuss how you've successfully managed studies from initiation to completion.
✨Showcase Your Leadership Skills
This role requires strong leadership, so prepare examples that highlight your ability to lead cross-functional teams. Think about times when you coordinated efforts between clinical, data, and regulatory teams to achieve study milestones. Demonstrating your leadership style will help you stand out.
✨Be Ready for Problem-Solving Scenarios
Expect questions that assess your problem-solving capabilities. Prepare to discuss specific challenges you've faced in previous studies and how you resolved them. This will show your potential employer that you can handle the fast-paced environment and unexpected issues that may arise.
✨Understand Regulatory Requirements
Since compliance is crucial in clinical studies, brush up on GCP and other relevant regulations. Be prepared to discuss how you’ve ensured compliance in past roles and how you manage vendor relationships to maintain quality standards. This knowledge will demonstrate your readiness for the role.