Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- 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 Gloucester 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 Gloucester
✨Tip Number 1
Before you even think about applying, make sure your LinkedIn profile is polished and reflects your experience in clinical studies. We want to see your achievements and skills shine through!
✨Tip Number 2
Networking is key! Reach out to professionals in the cardiovascular outcomes field. We can help you connect with others who might have insights or even leads on job openings.
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of GCP and SOPs. We recommend practising common interview questions related to study management and leadership to boost your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate candidates like you to join our team.
We think you need these skills to ace Clinical Study Lead - Cardiovascular Outcomes (CVO) in Gloucester
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 Leadership Skills: We want to see your leadership and communication skills shine through. Share examples of how you've led cross-functional teams or managed complex global studies, as this is crucial for the role.
Be Clear and Concise: When writing your application, keep it clear and to the point. Use bullet points where possible to make it easy for us to read and understand your qualifications and experiences quickly.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it helps us keep everything organised!
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 interactions with CROs. This will help demonstrate your capability to handle the responsibilities of the Clinical Study Lead position.
✨Ask Smart Questions
Come prepared with insightful questions about the company's approach to study delivery and how they manage relationships with vendors. This not only shows your interest but also gives you a chance to assess if the company aligns with your values and work style.
✨Practice Your Leadership Skills
Since this role involves leading geographically dispersed teams, think of scenarios where you've successfully aligned stakeholders across different functions. Practising how you communicate your leadership style can make a big difference in how you come across during the interview.