Job Description:
Medpace is the leading Contract Research Organization (CRO) for Biotech companies, continually adding Clinical Trial Managers of varying experience levels to its Clinical Trial Management Group in London.
Clinical Trial Managers with expertise in Oncology are welcome to continue working within their area of specialization or expand into a new therapeutic area.
We offer remote flexibility for those with relevant experience. Our competitive salary/bonus program, combined with equity grants, has proven highly rewarding for our associates.
Key Responsibilities:
* Manage and provide accountability for daily project operations, adhering to contracts and regulations such as ICH/GCP and applicable laws, rules, and regulations.
* Serve as primary Sponsor contact for operational project-specific issues and study deliverables.
* Maintain an in-depth understanding of protocol, therapeutic area, and indication.
* Oversee cross-functional internal project team members and deliverables, ensuring 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.
* Be responsible for managing study vendors.
* 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; an advanced degree in a health or life science-related field is preferred.
* Experience in Phases 1-4; Phases 2-3 are preferred.
* Minimum 5 years of Clinical Trial Management experience, CRO experience is preferred.
* At least 5 years of Project Manager/Clinical Trial Manager experience at a CRO is required for a remote-based role.
* Management of overall project timeline is essential.
* Bid defense experience is desirable.
* Strong leadership skills are required.
About Medpace:
Medpace is a full-service clinical contract research organization (CRO) providing 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 our scientific and disciplined approach.
We leverage local regulatory and therapeutic expertise across major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective.
Headquartered in Cincinnati, Ohio, we employ over 5,000 people across 40+ countries.
Why Choose 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 facing 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.
* Consistently 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.