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- Tasks: Lead clinical studies in cardiovascular outcomes and ensure compliance with company standards.
- Company: Dynamic healthcare organisation based in London, focused on innovative clinical research.
- Benefits: Competitive daily rate, flexible working arrangements, and opportunities for professional growth.
- Other info: 6-month contract with potential for further opportunities in a fast-paced environment.
- Why this job: Make a real difference in cardiovascular research while leading diverse teams.
- Qualifications: Experience in study delivery, particularly in cardiovascular outcomes, and strong leadership skills.
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 Chelmsford 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 Chelmsford
✨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 underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website for a smoother process! We’ve streamlined everything to make it easier for you to showcase your skills and experience. Plus, it gives us a chance to see your application first-hand!
We think you need these skills to ace Clinical Study Lead - Cardiovascular Outcomes (CVO) in Chelmsford
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 forget to mention your experience managing complex global studies and leading cross-functional teams. We love seeing candidates who can demonstrate their operational expertise and analytical skills!
Tailor Your Application: Customise your application for this specific role. Use keywords from the job description to show that you understand what we’re looking for. This helps us see you as a perfect fit for the Clinical Study Lead position!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into our hands quickly and efficiently. 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 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 involvement with Clinical Endpoint Committees. 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 CROs. 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 requires strong leadership and communication skills, think of scenarios where you've successfully aligned stakeholders or led a team through challenges. Practising how you articulate these experiences can make a big difference in how you come across during the interview.