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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 enhance your leadership skills in a fast-paced setting.
- Why this job: Make a real difference in cardiovascular health while leading impactful studies.
- Qualifications: Experience in study delivery and managing complex global trials.
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 Portsmouth 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 Portsmouth
✨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 ensure timely delivery.
✨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 Portsmouth
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 match the key accountabilities listed in the job description.
Showcase Your Skills: Don’t just list your qualifications; demonstrate how you've used them in past roles. If you’ve managed complex global studies or led cross-functional teams, share specific examples that illustrate your expertise.
Be Clear and Concise: We want to see your passion and qualifications, but keep it straightforward. Use clear language and avoid jargon unless it's relevant to the role. This helps us quickly understand your fit for the position.
Apply Through Our Website: For the best chance of success, make sure to apply through our website. This ensures your application goes directly to us and allows you to easily track your application status.
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. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easier for the interviewers to see your impact.
✨Ask Smart Questions
Come prepared with insightful questions about the company's approach to managing CROs or their strategies for site selection. This not only shows your interest but also demonstrates your understanding of the role's complexities.
✨Be a Team Player
Highlight your leadership and communication skills by discussing how you've aligned diverse stakeholder networks in previous projects. Emphasise your ability to collaborate effectively, as this is crucial for managing large, geographically dispersed teams.