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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 Stoke-on-Trent 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 Stoke-on-Trent
✨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 studies and maintain relationships with stakeholders.
✨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 Stoke-on-Trent
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 you've used them in past roles. We love seeing examples of your leadership and communication skills, especially in managing complex global studies.
Tailor Your Application: Customise your application for this specific role. Mention your familiarity with GCP and SOPs, and how you’ve successfully collaborated with CROs or other partners in previous projects. 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 for us to receive your application and ensures you’re considered for this exciting opportunity in London!
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 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 help you stand out during the interview.