Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical trials in cardiovascular, endocrine, and metabolic areas while ensuring compliance and quality.
- 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: Make a real impact on patients' lives while growing in a supportive and innovative environment.
- Qualifications: Bachelor's degree in health/life sciences; 5+ years of clinical trial management experience required.
- Other info: Join a company recognised by Forbes for its success and commitment to excellence.
The predicted salary is between 43200 - 72000 £ per year.
OverviewMedpace 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 OverviewMedpace 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 NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
#J-18808-Ljbffr
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 who have experience in cardiovascular, endocrine, or metabolic studies. Attend industry conferences or local meetups to make connections that could lead to job opportunities.
✨Tip Number 2
Familiarise yourself with Medpace's recent projects and achievements in the clinical trial space. This knowledge will not only help you understand their work better but also allow you to engage in meaningful conversations during interviews.
✨Tip Number 3
Highlight your leadership skills and project management experience in discussions. Medpace values strong leadership, so be prepared to share specific examples of how you've successfully managed teams and projects in the past.
✨Tip Number 4
Stay updated on the latest regulations and guidelines in clinical trials, particularly ICH/GCP standards. Demonstrating your knowledge of compliance can set you apart as a candidate who is ready to hit the ground running.
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 Medpace and how your values align with their mission.
Highlight Leadership Skills: Since the role requires strong leadership skills, provide examples of past experiences where you successfully led a team or managed a project. This will show your capability to oversee clinical trials effectively.
Showcase Relevant Certifications: If you have any certifications related to clinical trial management or good clinical practice (GCP), be sure to include them. 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
Be ready to provide specific examples of how you've managed clinical trials in the past. Highlight your experience with Phases 1-4, risk assessment, and vendor management to show that you can handle the responsibilities of the Clinical Trial Manager position.
✨Prepare for Behavioural Questions
Expect questions that assess your leadership and teamwork abilities. Use the STAR method (Situation, Task, Action, Result) to structure your answers, focusing on how you've successfully led teams and managed project timelines in previous roles.
✨Ask Insightful Questions
Prepare thoughtful questions about Medpace's approach to clinical trials, their company culture, and opportunities for professional growth. This shows your genuine interest in the company and helps you determine if it's the right fit for you.
