10.09.24 | Vollzeit | Basel (Basel-Stadt) | ACHIEVA Group Limited | CHF 103 - CHF 120 / Stunde Delivery of objectives. Act as a clinical expert in regulatory interfaces, investigator, and partner meetings. Lead the development of clinical documents (e.g., protocols, informed consent, reports). Offer medical leadership and input for strategic decisions, life cycle management, and trial
Später ansehen10.09.24 | Vollzeit | Basel (Basel-Stadt) | ACHIEVA Group Limited | CHF 65 - CHF 73 / Stunde Trial Scientist plays a pivotal role in the design, execution, and management of clinical trials. As a core member of the Clinical Trial Team, you will collaborate with physicians and crossfunctional teams to ensure the scientific integrity and smooth operation of trials. Your main responsibilities
Später ansehen30.08.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 125’000 - CHF 150’000 Studies and adequate monitoring. - In collaboration with data management secure the highest possible integrity and quality of the collected trial data. - Participate in the development and maintenance of medical science and clinical development specific global standards, processes, SOPs, quality control
Später ansehen30.08.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 80’000 - CHF 100’000 Entering IND preparing studies in the next few months. Our team is passionate about science and committed to improving patient outcomes through cutting-edge research and clinical trials. The Senior Scientist Nonclinical and Translational Development will be responsible for the coordination, execution
Später ansehen30.08.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 125’000 - CHF 150’000 Level strategic plans. - Collaborate with senior management to plan and budget for clinical trials. - Create and implement risk assessment and mitigation plans, performing regular reviews to continually assess for changes. - Engage with patient advocacy groups to help build patient-focused clinical
Später ansehen12.08.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 100’000 - CHF 125’000 Overall accountability for drug supply chain in preclinical and clinical trials. - Identify, select and manage appropriate Contract Development & Manufacturing Organizations (CDMOs) for appropriate development and manufacturing work of drug substance and drug product under cGMP. - Contribute to maintain
Später ansehen09.08.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 100’000 - CHF 125’000 Our passionate interest in fighting cancer. General Description The position will report to Distribution & Regional Quality, Europe Head. The Director IMP Quality Europe will provide GMP/GDP expertise and supervise the clinical trials supplies within the EU and Switzerland and ensure the correct
Später ansehen14.06.24 | Vollzeit | Basel (Basel-Stadt) | JobLeads GmbH | CHF 150’000 - CHF 200’000 But are not limited to protocol development, support study startup, oversight of trial execution, recruitment, ongoing clinical development management and closeout as appropriate. Compliance with internal processes, GCP/ICH and regulatory requirements, study and data monitoring, data analysis, are required
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