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For Companies At a Glance
- Tasks: Manage clinical trials, ensuring compliance and overseeing project operations.
- Company: Medpace is a leading CRO dedicated to advancing medical therapeutics globally.
- Benefits: Enjoy flexible work options, competitive pay, and generous PTO.
- Why this job: Make a real impact on patients' lives while growing in a supportive environment.
- Qualifications: Bachelor's degree in health/life sciences; 2+ years of clinical trial management experience required.
- Other info: Remote work available post-probation for experienced candidates.
The predicted salary is between 43200 - 72000 £ 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 the United Kingdom, specifically in London and Stirling. Clinical Trial Managers with expertise in Immunology and Infectious Diseases are welcome to continue to work in their area of expertise. We provide remote flexibility only with relevant experience (after probation). 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 2 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; and
- 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. #J-18808-Ljbffr
Clinical Trial Manager - UK (London, Stirling) - Infectious Disease / Immunology employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Manager - UK (London, Stirling) - Infectious Disease / Immunology
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical trials, especially in Immunology and Infectious Diseases. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in your field.
✨Tip Number 2
Network with professionals in the clinical trial management space, particularly those who have experience at CROs. Attend industry events or webinars to connect with potential colleagues and learn more about the company culture at Medpace.
✨Tip Number 3
Prepare to discuss specific examples of your project management experience, particularly in Phases 1-4 of clinical trials. Highlight any leadership roles you've taken on and how you've successfully managed timelines and deliverables.
✨Tip Number 4
Research Medpace's recent projects and achievements in the clinical trial sector. Being able to reference their work during your discussions will show your genuine interest in the company and its mission.
We think you need these skills to ace Clinical Trial Manager - UK (London, Stirling) - Infectious Disease / Immunology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, particularly in immunology and infectious diseases. Use specific examples to demonstrate your expertise in Phases 1-4 and any leadership roles you've held.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for the role and the impact of clinical trials on patient lives. Mention why you want to work with Medpace specifically and how your values align with theirs.
Highlight Relevant Skills: In your application, emphasise skills such as project management, risk assessment, and vendor management. Be sure to mention any experience with bid defense and your ability to lead cross-functional teams.
Proofread and Edit: Before submitting your application, thoroughly proofread all documents for spelling and grammatical errors. A polished application reflects attention to detail, which is crucial in clinical trial management.
How to prepare for a job interview at Medpace, Inc.
✨Know Your Protocols
Familiarise yourself with the specific protocols related to Immunology and Infectious Diseases. Being able to discuss these in detail will show your expertise and commitment to the role.
✨Demonstrate Leadership Skills
Prepare examples of how you've successfully led teams in previous projects. Highlight your ability to manage timelines and deliverables, as this is crucial for a Clinical Trial Manager.
✨Understand Regulatory Requirements
Brush up on ICH/GCP guidelines and any relevant laws. Showing that you have a solid understanding of compliance will reassure the interviewers of your capability to manage clinical trials effectively.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in past roles and how you overcame them, particularly in managing clinical trials.
