NHS and University Clinical Trial Professionals - Career Event: Clinical Trial Management – Medpace, London

University or NH S clinical research professional, considering a change to the Industry?   Medpace is delighted to host a recruitment event tailored to professionals working in an Academic setting or the NHS (Clinical Trial Managers, Clinical Research Coordinators, Clinical Research Nurses, Clinical Practitioners etc) to be considered for the Clinical Trial Manager position at Medpace.   This is a rare and exciting opportunity for clinical researchers seeking to make a switch into the industry !    Join the Medpace hiring team for an exclusive onsite event at our London Office to hear from former NHS and University-lead clinical research professionals who made the switch into the private industry and discover how to transform your career at a global CRO.   LOCATION: Central London DATE: Thursday 22nd October 2026 APPLICATION CLOSE DATE : Monday 19th October 2026     This is an opportunity for public sector professionals to enter the industry, to receive solid foundational training, work in an international environment, and accelerate their career in the research and development of cutting-edge therapeutics. Attendance at this event will act as a first step in eventually obtaining a position with us.   What to Expect Next: A member of our recruitment team will review your CV and Cover Letter and, if interested, you will be contacted for an RSVP.

Clinical Trial Manager: Manage and provide accountability for day-to-day operations of the studies conducted by Medpace on behalf of Biotech / Biopharma sponsors. Serve as primary Sponsor contact for operational project-specific issues and study deliverables Maintain in depth knowledge of protocol, therapeutic area, and indication Lead internal project team and p rovide cross-functional oversight of study team deliverables. Review and provide input for study protocol, database edit check specifications and final study report, when applicable Develop study-specific operational project plans Implement and manage a risk-based approach to project execution Responsible for management of study vendor s Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables, including CRA trip report review Qualifications Experience in clinical trials from a University setting and/or NHS (Clinical Trial Managers, Junior Doctors, Clinical Research Coordinators, Clinical Research Nurses, Clinical Practitioners etc). A background in one of our key therapeutic focus areas is a must: Oncology, Cardiovascular, Renal, Metabolic, Gastrointestinal.  Fluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international team Please include your cover letter in your application submission   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. Why Medpace? 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