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

trials.Main Responsibilities: • Leads a global team that supports all aspects of sample management for clinical trials of all phases. • Supports some aspects of the management of pre-clinical biospecimens. • Responsible for

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

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

across various medical disciplines. Your responsibilities will include ensuring the progress of each trial while engaging with clinical sites in coordination with the medical affairs team and Contract Research Organizations

facilitates clinical teamwork and communications to ensure timely attainment of trial milestones. • Ensures accuracy of reports and material work product. • Provides monthly billing information to finance team. • Presents at

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

, 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

. With 3000+ Clinical Trials carried out since 2012, Pratia brings tech-savvy, adaptable solutions in innovative treatments at Patients' convenience. Pratia is the platform, which connects Patients and Investigators with the

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

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

Studien (w/m/d) in Teilzeit (bis 50 %) Vertragsart: Befristet Beschäftigungsart: Teilzeit Bewerbung bis: 30.11.2025 • Unterstützung unseres Projektmanagement-Teams bei der Durchführung von klinischen Studien

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

, notifies the PM and SSU Manager and tracks out-of-scope work until it is assigned to back log. • Prepares the core submission documents and core clinical trial application dossier for amendments during life cycle maintenance of

systems, aiming to enhance treatment outcomes and patient satisfaction. • Partner with HCPs to refine patient pathways and treatment protocols in accordance with current clinical guidelines and industry best practices, thereby

systems, aiming to enhance treatment outcomes and patient satisfaction. • Partner with HCPs to refine patient pathways and treatment protocols in accordance with current clinical guidelines and industry best practices, thereby

-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. • Strategically plan and engage with national Key External Experts (KEEs) to maximize scientific exchange and

continuously develop deep expertise in oncology-related clinical and scientific literature to position both yourself and the team as trusted subject matter experts. • Strategically plan and engage with national Key External Experts

all SAS language, procedures and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH. Knowledge of SAS Enterprise Guide and/or SAS Studio is recommended