Jobs: clinical project manager

Clinical Project Manager49_744000012810675Obowiązki We are looking for a Project Manager with comprehensive experience to join our team at Eurofins bioskin in Hamburg. The Project Manager’s essential function is to organize and manage clinical studies coordinating all involved departments at Eurofins bioskin as well as external stakeholders...

The country Clinical Research Lead (CRL) responsibilities include operational delivery of strategic clinical studies assigned to the country, to support client';s pipeline, in accordance with ICH/GCP, client SOPs, local operating guidelines and local requirements, as applicable. CRL works locally, supporting Associate Director Clinical Operations (ADCO) /...

For our Clinical Trial Supply department in Marburg, King of Prussia or Zurich, we are looking for aClinical Trial Supply Study Manager (m/f/x)R-248394Fulltime / permanent The Clinical Trial Supply (CTS) Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the multi-year study lifecycle. The CTS Study Manager...

For our Clinical Trial Supply department in Marburg, King of Prussia or Zurich, we are looking for aClinical Trial Supply Study Manager (m/f/x)R-Fulltime / permanent The Clinical Trial Supply (CTS) Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the multi-year study lifecycle. The CTS Study Manager independently...

**JOB TITLE**:Clinical Operations Lead **LOCATION**:Netherlands, Canada, US, Germany, UK or Romania (Home-based) **REPORTS TO**: Manager, Monitoring & Site Management (Europe & Asia Pacific) **DEPARTMENT/UNIT NAME**: Monitoring & Site Management **JOB SUMMARY**: Responsible for the clinical operations of a project within a defined...

Zur Unterstützung suchen wir dich (m/w/d) ab sofort als Clinical Project Associate. Wir sind ein Dienstleistungsunternehmen, das sich auf die externe Projektunterstützung in der klinischen Medikamentenforschung spezialisiert hat. Zu unserem Kundenstamm zählen namhafte Großunternehmen aus den Branchen Pharma, Biotech und Forschung. Wir befinden uns in...

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description...

Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We...

For our Clinical Trial Supply department in Marburg, King of Prussia or Zurich, we are looking for aClinical Trial Supply Study Manager (m/f/x)R-248394Fulltime / permanentThe Clinical Trial Supply (CTS) Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the multi-year study lifecycle. The CTS Study Manager...

Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We...

MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,800 employees around the world. ...

For our Clinical Trial Supply department in Marburg, King of Prussia or Zurich, we are looking for a Clinical Trial Supply Study Manager (m/f/x) R-248394 Fulltime / permanent The Clinical Trial Supply (CTS) Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the multi-year study lifecycle. The CTS Study Manager...

Contract type: Permanent contract (part-time. From 2026, possibility of evolution to full-time depending on company needs and employee performance)Starting date: as soon as possibleThe Institut National du Cancer (INC) is a non-profit association established on June 25, 2015. The INC's mission is to contribute to the effective fight against cancer by...

Contract type: Permanent contract (part-time. From 2026, possibility of evolution to full-time depending on company needs and employee performance)Starting date: as soon as possibleThe Institut National du Cancer (INC) is a non-profit association established on June 25, 2015. The INC's mission is to contribute to the effective fight against cancer by...

You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: Welcome to our world At Sonova and Advanced Bionics, we create sense by bringing sound to life. Our innovative hearing care solutions help millions of people enjoy life's...

**Clinical Research Associate (M/F/d) for our German Team** **(level depending on experience)** *** **Job Purpose/Summary** As a CRA you will be responsible for the successful conduct of clinical trials and serve as main contact for the investigative site by representing CTI in a professional manner. **What You’ll Do** - Serve as main CTI contact for...

Kaia is a mission-focused health technology company. Our story began in 2016, when our founders Konstantin Mehl and Manuel Thurner, set out on a mission to bring affordable and accessible relief to millions of people with chronic conditions. No strangers to chronic pain themselves, they decided to innovate ways to remove the obstacles many people experience...

Your tasks: - Selection, qualification and training of external providers and clinical trial sites - Submission to regulatory authorities and Independent Ethics Committee/Institutional Review Board (IEC/IRB) - Support preparation of trial-specific documents, e.g. Informed Consent Form (ICF), submission document to IEC/IRB and regulatory authorities,...

**Job Purpose/Summary** As a CRA in Homeoffice you will be responsible for the successful conduct of clinical trials and serve as main contact for the investigative site by representing CTI in a professional manner. **What You’ll Do** - Conduct evaluation, initiation, monitoring and close out visits - Assist with regulatory and study start-up activities...

Als kompetenter Personaldienstleister bringt PERSONALHANSA seit über 35 Jahren Menschen in Arbeit. Mit Engagement und Expertise gelingt es uns die Interessen der Bewerber und unserer Kunden bestmöglich in Einklang zu bringen. PERSONALHANSA ist Mitglied der BAP/DGB Tarifgemeinschaft. Berufsanfänger und Berufserfahrene erhalten bei uns, neben sehr guten...