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For Companies At a Glance
- Tasks: Manage clinical trials and ensure project success while leading a dynamic team.
- Company: Join Medpace, a top CRO making a real difference in healthcare.
- Benefits: Enjoy competitive pay, flexible work, and great career growth opportunities.
- Why this job: Make an impact on patients' lives through innovative clinical research.
- Qualifications: 5+ years in clinical trial management; expertise in oncology or cardiovascular preferred.
- Other info: Be part of a supportive culture with recognition for excellence and employee appreciation.
The predicted salary is between 36000 - 60000 £ per year.
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.
- Strong leadership skills.
Company & Benefits
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 / Cardiovascular / Metabolic / GastroIntestinal indications 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.
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.
Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI) in City of Westminster employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI) in City of Westminster
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trial space, especially those who work at Medpace or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH/GCP guidelines and the specific therapeutic areas you're interested in. We want you to shine when discussing your experience and how it aligns with the role!
✨Tip Number 3
Showcase your leadership skills during interviews. Be ready to share examples of how you've managed teams and projects in the past. We love hearing about your successes and how you handle challenges!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always on the lookout for passionate Clinical Trial Managers like you to join our team.
We think you need these skills to ace Experienced Clinical Trial Manager (Oncology / Cardiovascular / Metabolic / GI) in City of Westminster
Some tips for your application 🫡
Know Your Stuff: Before you start writing, make sure you understand the role inside out. Familiarise yourself with the responsibilities and qualifications listed in the job description. This will help you tailor your application to show how your experience aligns perfectly with what we're looking for.
Be Specific: When detailing your experience, don’t just list your previous jobs. Use specific examples that highlight your skills in managing clinical trials, especially in Oncology, Cardiovascular, or other relevant areas. We want to see how you've tackled challenges and delivered results in your past roles.
Show Your Passion: Let your enthusiasm for the role shine through! Mention why you're excited about working with Medpace and how our mission resonates with you. A genuine passion for improving patient lives can really set your application apart from the rest.
Apply Through Our Website: We encourage you to submit your application directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re proactive and serious about joining our team!
How to prepare for a job interview at Medpace
✨Know Your Stuff
Make sure you have a solid understanding of the clinical trial process, especially in oncology, cardiovascular, metabolic, and GI areas. Brush up on ICH/GCP guidelines and be ready to discuss how you've applied these in your previous roles.
✨Showcase Your Leadership Skills
As a Clinical Trial Manager, you'll need to demonstrate strong leadership. Prepare examples of how you've successfully managed teams and projects in the past. Highlight any experience with cross-functional oversight and training, as this will resonate well with the interviewers.
✨Be Ready for Scenario Questions
Expect questions that ask how you would handle specific project challenges or risks. Think about past experiences where you had to manage timelines or vendor relationships, and be prepared to explain your thought process and decision-making.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the company culture, team dynamics, or upcoming projects. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
