At a Glance
- Tasks: Manage clinical trials and ensure project success in a dynamic environment.
- Company: Join Medpace, a leading CRO dedicated to advancing medical research.
- Benefits: Competitive salary, health benefits, remote work options, and career development.
- Other info: Enjoy a supportive culture with clear career paths and ongoing training opportunities.
- Why this job: Make a real impact in oncology while collaborating with top experts in the field.
- Qualifications: Bachelor's degree in health sciences and 2+ years of clinical trial management experience.
The predicted salary is between 54000 - 66000 £ 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.
- Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred.
- Management of overall project timeline.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence.
Collaborative Culture
Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. Leadership throughout Medpace is both accessible and approachable.
Continuous Growth & Development
- Office based environment with on-site mentors.
- Defined career paths with clear advancement opportunities.
- Industry renowned onboarding and training programs designed to accelerate professional development.
- Ongoing training and continuous learning opportunities throughout your career.
- An environment that encourages employees to influence change, contribute ideas, and grow quickly.
Other Employee Benefits
Competitive compensation programs that recognize and reward performance. Comprehensive health, wellness, retirement, and PTO benefits. Office based culture with occasional WFH that provides flexibility for eligible positions after training. Company-sponsored social events. Please note benefits may vary based on country.
Clinical Trial Manager (Oncology) in London employer: Medpace
Medpace is an exceptional employer, offering a collaborative and purpose-driven work environment in Cincinnati, Ohio, where employees can thrive alongside industry-leading experts in clinical research. With a strong focus on continuous learning and professional development, Medpace provides defined career paths, comprehensive benefits, and a culture that encourages innovation and employee contributions. Join us to make a meaningful impact on global health while enjoying competitive compensation and a supportive office-based atmosphere.
