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For Companies At a Glance
- Tasks: Lead clinical trials, manage projects, and ensure compliance with regulations.
- Company: Medpace is a top CRO dedicated to advancing medical research globally.
- Benefits: Enjoy flexible work options, competitive pay, and generous PTO.
- Why this job: Make a real impact on patients' lives while growing your career in a supportive environment.
- Qualifications: Bachelor's degree in health/life sciences; 2+ years in clinical trial management required.
- Other info: Remote work available after probation for experienced candidates.
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 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.
- 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.
- 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
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Clinical Trial Manager - UK (London, Stirling) - Infectious Disease / Immunology employer: Medpace
Contact Detail:
Medpace 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 developments in infectious diseases and immunology. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the field, making you a more attractive candidate.
✨Tip Number 2
Network with professionals in the clinical trial management space, especially those who work at Medpace or similar CROs. Attend industry conferences or webinars to connect with potential colleagues and learn about their experiences.
✨Tip Number 3
Prepare for the interview by practising common questions related to project management and clinical trials. Be ready to discuss specific examples from your past experience that highlight your leadership skills and ability to manage timelines effectively.
✨Tip Number 4
Research Medpace's recent projects and achievements in the clinical trial sector. Being able to reference their work during your conversation will show that you are proactive and genuinely interested in contributing to their 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 managing projects and leading teams.
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.
Highlight Relevant Experience: In your application, emphasise your experience in Phases 1-4 of clinical trials, especially if you have worked in a CRO environment. Include any bid defense experience and leadership roles you've held.
Proofread and Edit: Before submitting your application, thoroughly proofread your documents for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical trial management.
How to prepare for a job interview at Medpace
✨Know Your Protocols
Familiarise yourself with the specific protocols and regulations related to clinical trials, especially in immunology and infectious diseases. Being able to discuss these confidently will demonstrate your expertise and commitment to compliance.
✨Showcase Leadership Skills
Prepare examples that highlight your leadership experience, particularly in managing cross-functional teams. Medpace values strong leadership, so be ready to discuss how you've successfully led projects and resolved conflicts.
✨Discuss Risk Management
Be prepared to talk about your approach to risk assessment and management in clinical trials. Share specific instances where you identified potential risks and how you mitigated them to ensure project success.
✨Highlight Relevant Experience
Make sure to emphasise your experience in Phases 1-4 of clinical trials, particularly if you have worked at a CRO. Tailor your responses to reflect how your background aligns with the responsibilities outlined in the job description.