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- 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 remote work, competitive pay, bonuses, and equity grants.
- Why this job: Make a real impact on patients' lives while growing in a supportive environment.
- Qualifications: Bachelor's degree in health/life sciences; 5+ years of clinical trial management experience required.
- Other info: Join a recognised leader in the industry with a strong commitment to employee growth.
The predicted salary is between 36000 - 60000 £ per year.
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.
- 5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role.
- Management of overall project timeline; Bid defense experience preferred.
- 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.
Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - London employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. 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 about the latest trends.
✨Tip Number 2
Familiarise yourself with Medpace's mission and values. Understanding their approach to clinical trials and patient care will help you align your discussions during interviews and demonstrate your genuine interest in the company.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that showcase your leadership skills and project management capabilities. Highlight instances where you've successfully managed timelines and vendor relationships, as these are crucial for the role.
✨Tip Number 4
Stay updated on regulatory changes and best practices in clinical trial management. Being knowledgeable about ICH/GCP guidelines will not only boost your confidence but also show your commitment to maintaining high standards in clinical research.
We think you need these skills to ace Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - London
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Clinical Trial Manager position. Familiarise yourself with the specific areas of expertise mentioned, such as Cardiovascular, Endocrine, and Metabolic.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical trial management, particularly in the specified therapeutic areas. Emphasise your leadership skills and any experience with Phases 1-4 of clinical trials.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for the role and the impact of clinical research. Mention why you want to work at Medpace and how your values align with their mission.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical trial management.
How to prepare for a job interview at Medpace, Inc.
✨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 handled project timelines, risk assessments, and vendor management in previous roles.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world situations. Think of scenarios where you had to manage conflicts, ensure compliance with regulations, or lead a team through challenges, and be ready to share those experiences.
✨Emphasise Your Leadership Qualities
As a Clinical Trial Manager, strong leadership skills are crucial. Be prepared to discuss how you've motivated teams, provided training, and ensured high-quality deliverables in past projects. This will show that you can effectively lead a cross-functional team.
