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- Tasks: Lead clinical studies in cardiovascular outcomes and ensure compliance with company standards.
- Company: Dynamic healthcare organisation based in London, focused on innovative clinical research.
- Benefits: Competitive daily rate, flexible working arrangements, and opportunities for professional growth.
- Other info: 6-month contract with potential for future opportunities in a fast-paced environment.
- Why this job: Make a real difference in cardiovascular research while leading diverse teams.
- Qualifications: Experience in study delivery, particularly in cardiovascular outcomes, and strong leadership skills.
The location of the role is London. The duration of the contract is 6 months. The pay rate on offer is £650 - £700 per day (via Umbrella agency).
Key accountabilities of the role:
- Accountable to ensure all relevant studies follow company SOPs and GCP.
- With direction, may matrix with key Study conduct partners.
- Assist with maintaining relationships and monitor performance of CRO's and other vendors.
- With direction from Senior Clinical Staff, collaborate with Clinical Operations functional groups (Regional Monitoring, Data Management, and Operations Management) to ensure on time delivery of studies.
- Provide input into identifying implications of study progress upon overall timeline goals conduct plans.
- With oversight manage study start-up, conduct and close-out.
- Manage clinical trial material.
- Assist in the management of CRO's or other outsourcing partners as appropriate.
- Provide input into content and execution of investigator meetings / may present selected topics.
- Provide input into development of CRF.
- Provide input into site selection with coordinated input.
Key skills and experience:
- Experience in study delivery role (study leader or study manager) on cardiovascular outcomes study/ies (CVO).
- Managing complex global study footprints.
- Oversight of high site volumes (100-1,000+ sites).
- Leading cross-functional study teams.
- Experience with Clinical Endpoint Committees (CEC).
- Leading large, geographically dispersed teams.
- Scientific understanding (cardiovascular endpoints & populations).
- Operational expertise (large, global, long-term trials).
- Analytical skills (event-driven monitoring, data interpretation).
- Leadership & communication (alignment across complex stakeholder networks).
- Familiarity with: Data Monitoring Committees (DMC/DSMB).
Clinical Study Lead - Cardiovascular Outcomes (CVO) in Plymouth employer: Experis
Contact Detail:
Experis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Study Lead - Cardiovascular Outcomes (CVO) in Plymouth
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience with cardiovascular outcomes. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and SOPs. We want you to be able to discuss how you've ensured compliance in past studies. Show them you're not just a candidate, but the right candidate!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers. Focus on your experience managing complex global studies and leading cross-functional teams – these are key points they'll want to hear about.
✨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 familiar faces from our community, so make sure to highlight your relevant skills and experiences.
We think you need these skills to ace Clinical Study Lead - Cardiovascular Outcomes (CVO) in Plymouth
Some tips for your application 🫡
Keep It Relevant: Make sure your CV and cover letter highlight your experience in clinical study delivery, especially in cardiovascular outcomes. We want to see how your skills align with the role, so tailor your application to showcase your relevant expertise.
Showcase Your Leadership Skills: As a Clinical Study Lead, you'll be managing teams and collaborating with various stakeholders. Use your application to demonstrate your leadership experience and how you've successfully led cross-functional teams in the past.
Be Clear and Concise: When writing your application, clarity is key! Keep your language straightforward and avoid jargon unless it's relevant. We appreciate a well-structured application that gets straight to the point.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of being noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people!
How to prepare for a job interview at Experis
✨Know Your Stuff
Make sure you brush up on your knowledge of cardiovascular outcomes studies. Familiarise yourself with the key accountabilities mentioned in the job description, like GCP and SOPs. Being able to discuss these topics confidently will show that you're serious about the role.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've managed complex global studies or led cross-functional teams. Highlight your experience with high site volumes and any interactions with CROs. This will help demonstrate your capability to handle the responsibilities of the Clinical Study Lead position.
✨Ask Smart Questions
Come prepared with insightful questions about the company's approach to study delivery and how they manage relationships with vendors. This not only shows your interest but also gives you a chance to assess if the company aligns with your values and work style.
✨Be Ready to Discuss Challenges
Think about potential challenges you might face in this role, such as managing timelines or coordinating with geographically dispersed teams. Be ready to discuss how you would tackle these issues, showcasing your analytical skills and operational expertise.