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- Tasks: Lead complex clinical studies from start to finish, ensuring success and compliance.
- Company: Join a leading organisation in the cardiovascular research field, working remotely.
- Benefits: Competitive daily rate, flexible remote work, and a chance to make a real impact.
- Other info: Opportunity to collaborate with cross-functional teams and enhance your leadership capabilities.
- Why this job: Take ownership of groundbreaking studies and drive high-quality outcomes in a fast-paced environment.
- Qualifications: Proven experience as a Study Lead with strong project management skills.
The predicted salary is between 30000 - 40000 £ per year.
We are seeking an experienced Study Lead 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 established Study Lead experience who can confidently take ownership of study delivery and drive successful outcomes.
Key Responsibilities- Lead 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
- Proven experience as a Study Lead (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
- 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
Global Clinical Study Lead - Cardiovascular 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 Lead - Cardiovascular 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 on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on your leadership and project management skills. Be ready to share specific examples of how you've successfully led studies in the past, as this will show potential employers that you can hit the ground running.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds and shows your enthusiasm.
✨Tip Number 4
Apply through our website for the best chance at landing that Global Clinical Study Lead role. We’re all about making connections and helping you find the right fit, so don’t miss out on the opportunity to showcase your skills directly!
We think you need these skills to ace Global Clinical Study Lead - Cardiovascular in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Study Lead, especially in managing complex studies. We want to see how you've driven successful outcomes and met milestones in previous roles.
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 that align with our needs.
Showcase Your Teamwork Skills: Since this role involves coordinating cross-functional teams, make sure to mention your experience working with various stakeholders. We love seeing how you’ve fostered collaboration in past projects!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to hear from you!
How to prepare for a job interview at Carbon 60
✨Know Your Study Lifecycle
Make sure you can confidently discuss the full study lifecycle. Brush up on your experience with end-to-end study delivery, as this role requires you to take ownership of the entire process. Be ready to share specific examples of how you've successfully managed timelines, budgets, and milestones in previous studies.
✨Showcase Your Leadership Skills
This position demands strong leadership capabilities, so prepare to highlight your experience in leading cross-functional teams. Think of instances where you coordinated clinical, data, and regulatory teams to achieve a common goal. Demonstrating your ability to drive high-quality outcomes will set you apart.
✨Prepare for Regulatory Questions
Since compliance with regulatory requirements is crucial, be prepared to discuss your understanding of GCP or equivalent standards. Familiarise yourself with the latest regulations and be ready to explain how you've ensured compliance in past projects. This shows that you’re not just experienced but also up-to-date with industry standards.
✨Problem-Solving Scenarios
Expect to face questions about risk management and issue resolution. Prepare some scenarios where you successfully navigated challenges during a study. Highlight your problem-solving skills and how you managed stakeholder expectations while keeping the project on track.