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For Companies At a Glance
- Tasks: Lead clinical trials and ensure smooth project operations in a dynamic environment.
- Company: Join Medpace, a top CRO making a real difference in biotech.
- Benefits: Enjoy flexible work, competitive pay, and great career growth opportunities.
- Why this job: Make an impact on patients' lives while advancing your career in clinical research.
- Qualifications: 5+ years in Clinical Trial Management; expertise in Oncology is a plus.
- Other info: Be part of a passionate team dedicated to improving global health.
The predicted salary is between 36000 - 60000 £ per year.
Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. Clinical Trial Managers with expertise in Oncology or other therapy areas 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.
- 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 (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 like a pro! Reach out to your connections in the industry, especially those who work at Medpace or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by researching Medpace and its projects. Knowing their mission and recent achievements will help you stand out. Plus, it shows you're genuinely interested in being part of their team!
✨Tip Number 3
Practice your answers to common interview questions, especially those related to clinical trial management. We all know that confidence is key, so the more you rehearse, the better you'll perform when it counts.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're proactive and serious about joining the Medpace family.
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 is tailored to the Clinical Trial Manager role. Highlight your experience in managing clinical trials, especially in Oncology or other relevant therapy areas. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trial management and how your background makes you a great fit for Medpace. Keep it engaging and personal – we love to see your personality!
Showcase Relevant Experience: When filling out your application, be sure to showcase your experience in Phases 1-4 of clinical trials. If you've got any bid defense experience or leadership roles, make those stand out. We’re keen on seeing how you’ve led projects in the past!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and submit your details!
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 or any other therapeutic area you're familiar with. Brush up on ICH/GCP guidelines and be ready to discuss how you've applied them in your previous roles.
✨Showcase Your Leadership Skills
As a Clinical Trial Manager, you'll need strong leadership abilities. Prepare examples of how you've successfully managed teams and projects in the past. Highlight your experience in risk assessment and vendor management to demonstrate your capability.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to project management. Think about challenges you've faced in previous trials and how you overcame them. This will show your problem-solving skills and ability to think on your feet.
✨Ask Insightful Questions
Prepare thoughtful questions about Medpace's approach to clinical trials and their company culture. This not only shows your interest in the role but also helps you gauge if the company aligns with your values and career goals.
