mit internationalen Studiengruppen ist die AGO eine der stärksten Studiengruppen in der gynäkologischen Onkologie weltweit. Wir suchen für unsere Studiensekretariate in Wiesbaden und Essen Clinical Trial Manager / Studienkoordinatoren

. • Responsible for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials in the Therapeutic Area General Medicine • Function as the main point of contact

and tailor-made solutions • Close communication with colleagues from other departments/branches globally, working in a dynamic environment with teams from different geographies and levels • As an Account Manager, you

and tailor-made solutions • Close communication with colleagues from other departments/branches globally, working in a dynamic environment with teams from different geographies and levels • As an Account Manager, you

Mitarbeitende. Department Clinical Research The Clinical Research team is responsible for the implementation of all clinical research projects, from planning to reporting. Projects comprise clinical trials as well as all types of non

und Koordination von Investigator-initiated Trials (IITs) und Sammlung klinischer Daten • Bewertung von klinischen Studien und Daten sowie deren Auswirkung auf die medizinische Kommunikations- und Studienstrategie • Analyse

und internationalen Kongressen teil. • Du bist die Schnittstelle zwischen verschiedenen Fachabteilungen wie Clinical Trials, Produktmanagement, und Außendienst und schulst wissenschaftliche Inhalte nach innen und außen. • Du hast

upselling in key strategic accounts working in conjunction with Business Managers • Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines

device manufacturers. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results. Our new sales manager will collaborate directly with

, based on clinical trial experience, guidelines and SOPs • Responsible for certification of the centers, physicians and other related staff, as well as Edwards personnel and as outlined within Edwards' SOPs • Observe

• Collaborate with Regulatory Affairs and/or R&D on creation and review of regulatory (EMA and FDA) and clinical content and documentation, related to new drugs, clinical trials, as well as medical treatments (e.g. parts of clinical

apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity

efforts by providing regional insights relevant to clinical trial design, evidence generation, and reimbursement pathways • University degree in Health Economics, Public Health, Life Sciences, Pharmacy, Economics, or a

and Africa • Create appropriate training material and manage workshops, clinical trials and congresses independently • Help creating marketing material and content for marketing channels • Support the sales team and