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For Companies At a Glance
- Tasks: Lead clinical trials in cardiovascular, endocrine, and metabolic areas while managing project operations.
- Company: Medpace is a top CRO dedicated to advancing medical therapeutics globally.
- Benefits: Enjoy flexible work options, competitive pay, and generous PTO alongside wellness initiatives.
- Why this job: Join a passionate team making a real impact in healthcare with growth opportunities.
- Qualifications: Bachelor's degree in health/life sciences; 5+ years of clinical trial management experience required.
- Other info: Remote work available for experienced candidates; recognised by Forbes for excellence.
The predicted salary is between 43200 - 72000 £ per year.
Overview
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility only with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables
- Maintain in depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
- Develop operational project plans
- Manage risk assessment and execution
- Responsible for management of study vendor
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables
Qualifications
- Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred;
- Experience in Phases 1-4; Phases 2-3 preferred;
- Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred;
- Management of overall project timeline;
- Bid defense experience preferred; and
- Strong leadership skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America\\\’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - London employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - London
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those with experience in cardiovascular, endocrine, or metabolic areas. Attend industry conferences or webinars to connect with potential colleagues and learn more about the latest trends.
✨Tip Number 2
Familiarise yourself with Medpace's mission and values. Understanding their approach to clinical trials and their emphasis on safety and effectiveness will help you align your discussions during interviews with what they prioritise.
✨Tip Number 3
Prepare to discuss your previous experiences managing clinical trials, particularly in Phases 1-4. Be ready to provide specific examples of how you've handled project timelines, risk assessments, and vendor management.
✨Tip Number 4
Highlight your leadership skills and any experience you have in training or supervising team members. Medpace values strong leadership, so showcasing your ability to guide and support others will make you a more attractive candidate.
We think you need these skills to ace Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, particularly in the cardiovascular, endocrine, or metabolic fields. Use specific examples to demonstrate your expertise and achievements.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for clinical research. Mention why you are interested in working with Medpace and how your skills align with their mission.
Highlight Leadership Skills: Since strong leadership skills are essential for this role, provide examples of past experiences where you successfully led a team or managed a project. This will help showcase your ability to oversee cross-functional teams.
Showcase Relevant Certifications: If you have any certifications related to clinical trial management or project management, be sure to include them in your application. This can set you apart from other candidates and demonstrate your commitment to the field.
How to prepare for a job interview at Medpace
✨Know Your Therapeutic Area
Make sure you have a solid understanding of the cardiovascular, endocrine, and metabolic fields. Be prepared to discuss recent developments or challenges in these areas, as this will demonstrate your expertise and commitment to the role.
✨Showcase Your Project Management Skills
Highlight your experience managing clinical trials, especially in Phases 1-4. Be ready to provide specific examples of how you've successfully managed timelines, budgets, and team dynamics in previous roles.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world situations. Think about past challenges you've faced in clinical trial management and how you overcame them, particularly in relation to risk assessment and vendor management.
✨Emphasise Leadership Experience
Since strong leadership skills are crucial for this role, be prepared to discuss your leadership style and experiences. Share examples of how you've motivated teams, resolved conflicts, and ensured project deliverables were met.
