Overview
Medpace Stirling, Scotland, United Kingdom is seeking a Clinical Trial Manager (Associate Director) to join the Clinical Trial Management Group in Stirling. Medpace is a leading CRO for biotech companies, and the role supports oncology and other therapy areas. Remote flexibility is offered only with relevant experience. We provide a competitive salary/bonus program, plus equity grants.
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, including 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 preferred
* Experience in Phases 1-4; Phases 2-3 preferred
* Minimum of 5 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
* 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 a 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, 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 diseases across 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
What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Seniority level
* Not Applicable
Employment type
* Full-time
Job function
* Research, Analyst, and Information Technology
* Industries
* Pharmaceutical Manufacturing
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