2024. 05. 22. | Teljes munkaidõ | Budapest | ParexelWill actively lead the Parexel and client teams by combining your deep clinical research experience with insight into client pressures in order to develop the right solution for the will provide overall cross-functional leadership of our clinical trials and studies as well as the project teams
Nézze később2024. 05. 22. | Teljes munkaidõ | Budapest | ParexelWhen our values align, there's no limit to what we can achieve. We are currently looking for experienced Project Quality and Risk Leads with expertise with ICH-GxP principles and clinical trial regulations to be based in Romania or Poland or Lithuania or Hungary or Spain or Turkey .As the Senior
Nézze később2024. 05. 22. | Teljes munkaidõ | Budapest | ParexelQueriesCollaborates with primary Site Manager who will act as the primary liaison with site personnelThe IndividualA minimum of 1 year experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite)Bachelor’s degree or Registered Nurse (RN) in a related field or equivalent combination
Nézze később2024. 05. 19. | Teljes munkaidõ | Budapest | ParexelAre accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through
Nézze később2024. 05. 02. | Teljes munkaidõ | Budapest | ParexelLithuania, Czechia, Serbia and the Senior Regulatory Affairs Associate you will come with a few years of Regulatory Affairs experience gained in the industry. You will bring experience in Clinical Trial Applications (CTA) from various European locations. You will have a chance to work
Nézze későbbNe hagyja ki a munkát!
Napi új bejegyzéseket kaphat e-mailben a Clinical Trial Manager Budapesti Megye.