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- Tasks: Lead clinical studies in cardiovascular outcomes and ensure compliance with regulations.
- Company: Dynamic healthcare company based in London, focused on innovative research.
- Benefits: Competitive daily rate, flexible working arrangements, and professional growth opportunities.
- Other info: Join a collaborative team and work on global projects with significant impact.
- Why this job: Make a real difference in cardiovascular health while leading impactful studies.
- Qualifications: Experience in clinical study management, especially in cardiovascular outcomes.
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 CROs 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 CROs 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 Yorkshire 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 Yorkshire
✨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 fit for their team!
✨Tip Number 3
Don’t forget to showcase your leadership skills! Be ready to share examples of how you've led cross-functional teams or managed high site volumes. This is your chance to shine and demonstrate your operational expertise.
✨Tip Number 4
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. Let’s get you that Clinical Study Lead role!
We think you need these skills to ace Clinical Study Lead - Cardiovascular Outcomes (CVO) in Yorkshire
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Study Lead role. Highlight your experience in cardiovascular outcomes studies and any relevant leadership roles you've held. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background makes you the perfect fit. Don't forget to mention your experience with managing complex global studies!
Showcase Your Skills: In your application, be sure to showcase your analytical skills and operational expertise. We love candidates who can demonstrate their understanding of clinical endpoint committees and data monitoring. Make it clear how you can contribute to our team!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss out on any important updates. Plus, it’s super easy!
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 latest trends and challenges in the field, as well as the specific methodologies used in clinical trials. This will show that you're not just interested in the role but also passionate about the subject matter.
✨Showcase Your Leadership Skills
As a Clinical Study Lead, you'll need to demonstrate your ability to lead cross-functional teams. Prepare examples from your past experiences where you've successfully managed teams or projects, especially in complex global settings. Highlight your communication skills and how you've aligned stakeholders in challenging situations.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to study management and oversight. Think about how you would handle high site volumes or manage relationships with CROs. Practising these scenarios can help you articulate your thought process and decision-making skills effectively.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the company’s approach to managing large-scale trials or how they ensure compliance with GCP. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your career goals.