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For Companies At a Glance
- Tasks: Lead clinical trials, manage project operations, and ensure compliance with regulations.
- Company: Medpace is a top CRO, driving innovation in biotech and improving patient lives globally.
- Benefits: Enjoy flexible work options, competitive pay, equity grants, and generous PTO.
- Why this job: Make a real impact on healthcare while growing your career in a supportive environment.
- Qualifications: Bachelor's degree in health/life sciences; 5+ years in clinical trial management required.
- Other info: Join a recognised leader in the industry with a strong commitment to employee growth.
The predicted salary is between 48000 - 84000 £ 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 Oncology 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?
- 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.
EO/AA Employer M/F/Disability/Vets
Clinical Trial Manager (Associate Director) - London employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager (Associate Director) - London
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience with CROs. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in oncology and clinical trials.
✨Tip Number 2
Familiarise yourself with Medpace's specific projects and therapeutic areas. Understanding their recent studies and successes can help you tailor your conversations during interviews and demonstrate your genuine interest in their work.
✨Tip Number 3
Prepare to discuss your leadership experiences in detail. Since strong leadership skills are crucial for this role, think of specific examples where you've successfully managed teams or projects, particularly in a clinical setting.
✨Tip Number 4
Stay updated on regulatory changes and best practices in clinical trial management. Being knowledgeable about ICH/GCP guidelines and how they apply to your work will show that you're proactive and well-prepared for the responsibilities of the role.
We think you need these skills to ace Clinical Trial Manager (Associate Director) - London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, especially in oncology if applicable. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trials and your leadership skills. Mention specific experiences that align with the responsibilities outlined in the job description.
Highlight Relevant Qualifications: Clearly state your educational background and any advanced degrees in health or life sciences. Emphasise your years of experience in clinical trial management and any specific phases you have worked on.
Showcase Your Leadership Skills: Provide examples of how you've successfully managed teams and projects in the past. Highlight your ability to oversee cross-functional teams and ensure project deliverables are met.
How to prepare for a job interview at Medpace
✨Know Your Protocols
Familiarise yourself with the specific protocols and therapeutic areas relevant to the role. Being able to discuss these in detail will demonstrate your expertise and commitment to the position.
✨Showcase Leadership Skills
Prepare examples of how you've successfully led teams in previous roles. Highlight your ability to manage cross-functional teams and ensure project deliverables are met, as this is crucial for a Clinical Trial Manager.
✨Understand Risk Management
Be ready to discuss your experience with risk assessment and management in clinical trials. Providing concrete examples of how you've navigated challenges will show your problem-solving skills and strategic thinking.
✨Ask Insightful Questions
Prepare thoughtful questions about Medpace's projects, culture, and future directions. This not only shows your interest in the company but also helps you gauge if it's the right fit for you.