Executive Director Clinical Development
... , Company Core Data Sheet, Annual Safety Report IND (Investigational New Drug) Safety Reports. Thanks to your expertise, ...
... , Company Core Data Sheet, Annual Safety Report IND (Investigational New Drug) Safety Reports. Thanks to your expertise, ...
... , Company Core Data Sheet, Annual Safety Report IND (Investigational New Drug) Safety Reports. Thanks to your expertise, ...
... and development of cutting edge drugs, where you can grow your ... is an asset; Knowledge of drug development, clinical trial management and ...
... Access Programs to safeguard participant safety, data accuracy, and protocol adherence. ... trial design, regulatory standards, and drug development. Proficient in Microsoft Office ( ...
... with key opinion leaders and physicians, overseeing Clinical Affairs investments and ... on GCP adherence and patient safety. Collaborate on risk management activities ...
... to accelerate the development of drugs and devices that save lives ...
Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the DACH region, specifically in Munich, Germany. Clinical Trial Managers with ...
Medpace 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 Clinical Trial ...
Medpace 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 Clinical Trial ...
The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study ...