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- Tasks: Lead clinical studies in cardiovascular outcomes and ensure compliance with regulations.
- Company: Dynamic healthcare company focused on innovative cardiovascular research.
- Benefits: Competitive daily rate, flexible working arrangements, and professional growth opportunities.
- Other info: Join a collaborative environment with opportunities for career advancement.
- Why this job: Make a real difference in cardiovascular health while leading impactful studies.
- Qualifications: Experience in managing cardiovascular studies and leading cross-functional teams.
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).
Locations
Clinical Study Lead - Cardiovascular Outcomes (CVO) in Devon, 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 Devon, 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 referrals.
✨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 in the process. Let’s get you that Clinical Study Lead role!
We think you need these skills to ace Clinical Study Lead - Cardiovascular Outcomes (CVO) in Devon, Plymouth
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 skills that match the job description. We want to see how your background aligns 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 experience makes you the perfect fit. Don’t forget to mention your familiarity with managing complex global studies and leading cross-functional teams.
Showcase Your Achievements: When detailing your experience, focus on specific achievements rather than just duties. For instance, if you've successfully managed high site volumes or led large teams, share those successes! We love to see quantifiable results.
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 the role. Plus, it shows you’re keen on joining our team at StudySmarter!
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 not only help you answer questions confidently but also show your genuine interest in the role.
✨Showcase Your Leadership Skills
As a Clinical Study Lead, you'll need to demonstrate strong leadership abilities. Prepare examples from your past experiences where you've successfully led cross-functional teams or managed complex study footprints. Highlight how you navigated challenges and ensured timely delivery of studies.
✨Understand the Company’s SOPs and GCP
Familiarise yourself with the company's standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines. Be ready to discuss how you’ve adhered to these in previous roles and how you plan to ensure compliance in this position.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare insightful questions about the company’s approach to managing CROs, their expectations for the role, and how they measure success. This shows that you're not just interested in the job, but also in how you can contribute to their goals.