Oncology PhD to CTM: Associate Clinical Trial Manager

Job Summary Medpace is currently seeking candidates with Oncology related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, LyonClinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial...

Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, Lyon Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial...

A clinical contract research organization is seeking an Associate Clinical Trial Manager in Lyon, France. This role is ideal for recent PhD graduates in Life Sciences, offering foundational training and career development in clinical project management. Responsibilities include collaborating on study activities, maintaining project reports, and ensuring...

Job SummaryMedpace is currently seeking candidates with Renal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, Lyon Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial...

A clinical research organization located in France seeks an Associate Clinical Trial Manager to join their Lyon office. This full-time role is excellent for recent PhD graduates looking to start their careers with foundational training in clinical project management. Responsibilities include communicating on global study activities, maintaining project...

Assist the clinical team in the filing, tracking, and archiving of clinical documentation.Perform regular quality control (QC) checks on TMF documentation to ensure accuracy, consistency, and compliance with applicable regulatory and internal standards.Manage the timely update of TMF/eTMF documentsParticipate in the creation and maintenance of essential...

Dermatology We are seeking several Medical Directors to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a...

Dermatology We are seeking several Medical Directors to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a...

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. NAMSA has been a key contributor to the development of the test...