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- Tasks: Lead clinical studies in cardiovascular outcomes and ensure compliance with regulations.
- Company: Dynamic healthcare company focused on innovative clinical research.
- Benefits: Competitive daily rate, flexible working environment, and professional growth opportunities.
- Other info: Join a collaborative team and work on global projects in a fast-paced environment.
- Why this job: Make a real difference in cardiovascular health while leading impactful studies.
- Qualifications: Experience in clinical study delivery and strong leadership skills required.
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 Cardiff 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 Cardiff
✨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! During interviews, share specific examples of how you've led cross-functional teams or managed high site volumes. This will help you stand out as a candidate who can handle the complexities of global studies.
✨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 Cardiff
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 key accountabilities of the role.
Showcase Your Skills: Don’t just list your qualifications; demonstrate how your analytical skills and operational expertise have led to successful study outcomes in the past. We love seeing real examples!
Tailor Your Application: Customise your application for this specific role. Mention your familiarity with GCP and SOPs, and how you’ve managed complex global studies before. This helps us see you as a perfect fit!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands quickly. Plus, it shows us you’re keen on joining our team!
How to prepare for a job interview at Experis
✨Know Your Stuff
Make sure you brush up on your knowledge of cardiovascular outcomes studies. Be ready to discuss specific examples from your past experience that demonstrate your understanding of the complexities involved in managing large-scale trials.
✨Showcase Your Leadership Skills
Prepare to talk about your experience leading cross-functional teams. Think of instances where you successfully aligned stakeholders or managed conflicts, as this role requires strong leadership and communication skills.
✨Understand the Bigger Picture
Familiarise yourself with the company’s SOPs and GCP guidelines. Be prepared to discuss how you would ensure compliance while managing study timelines and deliverables, as this is crucial for the role.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical trials and their expectations for the Clinical Study Lead. This shows your genuine interest in the role and helps you assess if it’s the right fit for you.