ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to

for use in cancer treatment. We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone

Title: Clinical Study Lead Company: Multi-Asset Biotechnology Company Location: Germany Apsida is working with an exciting, growing biotech in Germany who are expanding their Clinical Team. The company are developing

affiliates in 13 European countries and Canada. For our development and production site in Pfaffenhofen/Ilm we are seeking highly qualified candidates to fill the position: Manager (m/f/x) Systems Clinical Supply Planning

affiliates in 13 European countries and Canada. For our development and production site in Pfaffenhofen/Ilm we are seeking highly qualified candidates to fill the position: Manager (m/f/x) Systems Clinical Supply Planning

Oracle Life Sciences is a leader in cloud technology, pharmaceutical research, and consulting, trusted globally by professionals in both large and emerging companies engaged in clinical research and pharmacovigilance

iOmx Therapeutics is a clinical-stage company in the field of immuno-oncology located in Martinsried/Munich, Germany. We are focusing on the development of first-in-class cancer immunotherapies, addressing novel immune

iOmx Therapeutics is a clinical-stage company in the field of immuno-oncology located in Martinsried/Munich, Germany. We are focusing on the development of first-in-class cancer immunotherapies, addressing novel immune

für die Herstellung von klinischen Prüfpräparaten (IMP) und die termingerechte Lieferung (inkl. Bestellprozessen) der IMP an die Prüfzentren inklusive deren Etikettierung, Verpackung und Lieferung Übernahme aller anfallenden Logistikthemen

Dich jetzt! • Du bist verantwortlich für die Qualität unserer Arzneimittelstudien – dabei stellst Du die Einhaltung von GCP Vorgaben und angrenzender Regularien bei uns, unseren Vendoren und unseren Prüfzentren sicher. • Du leitest unser Clinical Quality

für die Herstellung von klinischen Prüfpräparaten (IMP) und die termingerechte Lieferung (inkl. Bestellprozessen) der IMP an die Prüfzentren inklusive deren Etikettierung, Verpackung und Lieferung Übernahme aller anfallenden Logistikthemen

Scientific IT-Manager – Clinical Research (m/w/d) 102351 • Vollzeit • München • Home-Office-OptionenWir sind Helmholtz Munich. In einer sich schnell verändernden Welt entwickeln wir bahnbrechende Lösungen

Scientific IT-Manager – Clinical Research (m/w/d) 102351 • Vollzeit • München • Home-Office-OptionenWir sind Helmholtz Munich. In einer sich schnell verändernden Welt entwickeln wir bahnbrechende Lösungen

for use in cancer treatment. We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone

for use in cancer treatment. We are developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing cancers such as neuroendocrine cancers or bone

Medicover Integrated Clinical Services (MICS), als spezialisierte Geschäftseinheit innerhalb der Division Diagnostic Services, besteht aus mehr als 200 engagierten Mitarbeitern. Unser Fokus liegt auf klinischen Studien

Scientist Clinical (gn) as Medical Doctor wanted Our client aspires to emulate the innovation and disruption akin to Tesla within the pharmaceutical industry. They aim to astonish Big Pharma by showcasing the boundless

in company sponsored studies and engaging with clinical study sites, study personnel, Key Opinion Leaders (KOLs), and other health care providers with scientific exchange and clinical support. The MSL functions as a regional

Präzisionspsychiatrie zum nächstmöglichen Zeitpunkt, in Teilzeit, eine Study Nurse (m/w/d) • Ziel: Umsetzung klinischer Studien nach internationalen Standards • Koordination und Organisation unserer klinischen Studien

und Clinical Trial Regulation (CTR) für klinische Prüfpräparate entsprechen • Entscheidung über Freigabe bzw. Zurückweisung von Ausgangsstoffen, Verpackungsmaterial, Zwischenprodukten, Bulkware und endverpackten Prüfpräparaten