Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is
Job SummaryMedpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the
Job SummaryThis position is office based in Munich, Germany.What can Medpace offer you?Flexible working conditions – Hybrid working model and flexible working hoursCompetitive employee benefitsAnnual Merit increasesCasual Dress CodeResponsibilitiesLine management of Clinical Research Associates (CRAs)RecruitmentInvolvement in
Job SummaryDue to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and engage in clinical trial management on a day-to-day
Job SummaryMedpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the
Overview In this role you support the Clinical Safety team to advance safety activities for global trials. You will work with Medical Monitors, QA, and trial managers to process SAE reports, generate safety narratives, and ensure
Overview In this role, you will lead clinical trial operations for sponsor-specific partnerships in Germany, overseeing site and central monitoring with a focus on patient safety and data integrity. You will collaborate with cross-functional teams to
Overview As a Senior Contract Associate, you drive the drafting, negotiation, and finalization of complex Clinical Site Contracts for clinical trials. You will serve as the liaison between CBO, GCO, Legal, sites, and external providers to
Overview In this role you enable high-quality, compliant clinical monitoring as a senior CRA within a global, cross-functional team. You lead site oversight, support study recruitment and training, and drive adherence to SOPs, ICH GCP, and
Overview In this role you will support global clinical trial management activities within a cross-functional team. You will apply your analytical and academic training to project administration, helping to accelerate development of therapeutics. This is an
Overview In this role you will join the Clinical Trial Management team to support global trial operations and planning. You’ll apply analytical and academic skills to manage clinical project administration in an international setting. The position
Overview In this role based in Munich, you will lead and develop Clinical Research Associates (CRAs) to support Medpace’s global clinical trials. You work closely with CTMs and training teams to ensure high performance, staffing, and project
Overview In this role you help drive clinical trial management within Medpace’s German team, supporting timely, accurate task delivery and cross-functional coordination. You will manage project documentation, timelines, and site logistics, collaborating with sponsors, sites, and