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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 managing cardiovascular studies and strong leadership skills required.
The predicted salary is between 130000 - 140000 £ per year.
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 Stevenage 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 Stevenage
✨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 all know that confidence is key, so practice answering common questions related to study management and your experience with CROs.
✨Tip Number 3
Showcase your leadership skills! Be ready to discuss how you've led cross-functional teams in the past. Use specific examples to highlight your ability to manage complex global studies and keep everyone aligned.
✨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 and engaged in their job search.
We think you need these skills to ace Clinical Study Lead - Cardiovascular Outcomes (CVO) in Stevenage
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. Tailor your application to show how your skills align with the key accountabilities of the Clinical Study Lead role.
Showcase Your Skills: Don’t just list your qualifications; demonstrate how you've used them in past roles. Talk about your experience managing complex global studies and leading cross-functional teams to give us a clear picture of your capabilities.
Be Clear and Concise: We appreciate straightforward applications! Use clear language and avoid jargon where possible. Make it easy for us to see why you’re the right fit for the role without wading through unnecessary fluff.
Apply Through Our Website: For the best chance of success, make sure to apply directly through our website. This helps us keep track of your application and ensures you’re considered for the Clinical Study Lead position in London.
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 involvement with Clinical Endpoint Committees. This will help demonstrate your fit for the position.
✨Ask Smart Questions
Come prepared with insightful questions about the company's approach to study delivery and how they manage relationships with CROs. This not only shows your interest but also gives you a chance to assess if the company aligns with your career goals.
✨Practice Your Leadership Skills
Since this role involves leading geographically dispersed teams, be ready to discuss your leadership style. Think of scenarios where you've successfully aligned stakeholders across complex networks and be prepared to share those stories during the interview.