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- Tasks: Lead global clinical studies in cardiovascular research and ensure successful delivery.
- Company: Join a leading organisation in the healthcare sector with a focus on innovation.
- Benefits: Competitive daily rate, remote work flexibility, and valuable industry experience.
- Other info: Opportunity to work with cross-functional teams and enhance your professional network.
- Why this job: Make a real difference in healthcare while developing your leadership skills.
- Qualifications: Proven experience as a Study Lead and strong project management skills.
The predicted salary is between 30000 - 40000 £ per year.
Do not pass up this chance, apply quickly if your experience and skills match what is in the following description.
Type: Temporary
Duration: 12 months (tbc)
Location: Remote (client based in London)
Rate: circa. £(Apply online only) per day (via Umbrella, INSIDE IR35)
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
Contact Detail:
Carbon 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 or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your project management skills and understanding of clinical trial processes. Be ready to discuss how you've successfully led studies in the past and how you handle challenges.
✨Tip Number 3
Showcase your leadership abilities! During interviews, share specific examples of how you've coordinated cross-functional teams and managed stakeholder relationships. This will highlight your fit for the Global Clinical Study Lead role.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
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 is tailored to the Global Clinical Study Lead role. Highlight your experience in leading studies and managing cross-functional teams, as these are key aspects of the job.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your past successes in study delivery and how you’ve navigated challenges in clinical environments.
Showcase Your Skills: Don’t forget to emphasise your project management and leadership skills. We want to see how you’ve effectively managed stakeholders and ensured compliance with regulatory standards in your previous roles.
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’re considered for this exciting opportunity!
How to prepare for a job interview at Carbon
✨Know Your Study Lifecycle
Make sure you can confidently discuss your experience with the full study lifecycle. Be prepared to share specific examples of how you've led studies from start to finish, highlighting any challenges you faced and how you overcame them.
✨Showcase Your Leadership Skills
Since this role requires strong leadership, think of instances where you've successfully managed cross-functional teams. Prepare to explain how you coordinated efforts between clinical, data, and regulatory teams to achieve project goals.
✨Understand Regulatory Requirements
Brush up on GCP and other relevant regulations before the interview. Being able to discuss compliance and quality standards will show that you’re not just a great leader but also someone who understands the importance of adhering to industry guidelines.
✨Prepare for Stakeholder Management Questions
Expect questions about managing multiple stakeholders. Have examples ready that demonstrate your communication skills and how you’ve navigated differing priorities to keep everyone aligned and satisfied.