19.09.24 | Vollzeit | Morges | JobLeads GmbH | CHF 150’000 - CHF 200’000 Responsible person at EU level for named patient programs and Regional Medical Affairs sponsored trials. 6. Be accountable for Medical affairs budget related to EU HQ driven Medical Affairs events or programs. 7. Actively leads the collaboration between Global & EU Regional Medical Affairs/Clinical
Später ansehen16.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 80’000 - CHF 100’000 You will also participate in the optimal implementation of the clinical studies under the supervision of the clinical affairs manager. The primary activities include but are not limited to Biology Activities - Perform in vivo experiments to understand the in vivo biological processes taking place
Später ansehen15.09.24 | Vollzeit | Morges | JobLeads GmbH | CHF 150’000 - CHF 200’000 Activities for assigned products. - Ensure local and global risk management plan preparation and execution throughout a medicinal product’s lifecycle. - Formulate clinical trial and postmarketing risk management safety strategies that are in alignment with the company's drug development and commercialization
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Contribute to CRO/Vendor selection and qualification process, assess relevant CROs procedures during selection process to establish a pro-active quality approach, guaranteeing compliance with regulatory requirements. 3. Collaborate with the Clinical Trial Manager and other Functional Area Representatives
Später ansehen29.08.24 | Vollzeit | Morges | JobLeads GmbH | CHF 150’000 - CHF 200’000 Familiarity with GCP/ICH/FDA requirements as well as clinical trial design, biostatistics, medical writing, product safety, healthcare compliance and regulatory affairs. - Strong interpersonal, verbal and written communication skills. Strong public speaking skills. - Excellent leadership and management skills
Später ansehen25.08.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Vendor selection and qualification process, assess relevant CROs procedures during selection process to establish a pro-active quality approach, guaranteeing compliance with regulatory requirements - Collaborate with the Clinical Trial Manager and other Functional Area Representatives in the Study Team
Später ansehen12.08.24 | Vollzeit | Vevey | JobLeads GmbH | CHF 80’000 - CHF 100’000 Agreements, university research agreements, service agreements, trials agreements, material transfer agreements, clinical trials agreements, patent acquisitions, in-licensing and out-licensing agreements), balancing speed of execution with adequate protection; 6. Coordinate with contract managers, scientists
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