At a Glance
- Tasks: Manage clinical trials and ensure project success while collaborating with diverse teams.
- Company: Join Medpace, a leading CRO making a real impact in biotech.
- Benefits: Enjoy flexible work, competitive pay, bonuses, and career growth opportunities.
- Other info: Recognised by Forbes for excellence and offers a supportive work culture.
- Why this job: Be part of a mission to improve lives through innovative medical research.
- Qualifications: Bachelor's degree in health/life sciences and 5+ years of clinical trial management experience.
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 Nephrology 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 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 employer: Medpace
Join our dynamic Clinical Operations team in London, where we prioritise employee growth and foster a collaborative work culture. As a Clinical Trial Site Relationship Coordinator, you'll benefit from ongoing professional development opportunities while working in a vibrant environment that values strategic relationships and innovative solutions in clinical research. Enjoy the unique advantage of reduced travel while making a meaningful impact in the field of clinical trials.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Manager
✨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 lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by researching Medpace's projects and values. Show us you’re not just another candidate; demonstrate your passion for clinical trials and how your experience aligns with their mission.
✨Tip Number 3
Practice your pitch! Be ready to explain how your background in Nephrology or other therapeutic areas makes you the perfect fit for the Clinical Trial Manager role. Confidence is key!
✨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 serious about joining the Medpace team.
We think you need these skills to ace Clinical Trial Manager
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 Nephrology if applicable. 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 trials and how your background makes you a great fit for Medpace. We love seeing enthusiasm and a personal touch.
Showcase Relevant Experience:When filling out your application, be sure to showcase your relevant experience in Phases 1-4 of clinical trials. We’re particularly interested in your leadership skills and any vendor management experience you have.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensure it gets into the right hands. Plus, it shows you’re 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 relation to ICH/GCP guidelines. Brush up on your knowledge of nephrology if that's your area of expertise, or be ready to discuss how you can adapt to new therapeutic areas.
✨Showcase Your Leadership Skills
As a Clinical Trial Manager, you'll need to demonstrate strong leadership abilities. Prepare examples from your past experiences where you've successfully managed teams or projects, highlighting your ability to oversee cross-functional teams and ensure project deliverables are met.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills and risk management strategies. Think of specific scenarios where you've had to manage project timelines or vendor relationships, and be prepared to discuss how you handled challenges effectively.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in Medpace and the role. Inquire about their approach to clinical trials, team dynamics, or opportunities for professional growth within the company. This shows you're genuinely interested and engaged.
