18.06.24 | Vollzeit | München | JobLeads GmbH | 125.000 € - 150.000 € Parts of Niedersachsen Key Responsibilities - Creating and forming programs out of the medical strategy within their designated scope, schedule, and resources - Management of all medical affairs activities in territory - Development, implementation, and project lead of medical scientific projects
Später ansehen17.06.24 | Vollzeit | München | JobLeads GmbH | 125.000 € - 150.000 € Parts of Niedersachsen Key Responsibilities - Creating and forming programs out of the medical strategy within their designated scope, schedule, and resources - Management of all medical affairs activities in territory - Development, implementation, and project lead of medical scientific projects
Später ansehen17.06.24 | Vollzeit | Gräfelfing | Immunic AGStrategic recommendations to meet project goals. Develop and refine clinical protocols, overseeing medical monitoring and ongoing medical data review, including protocol exemptions, violations, and eligibility issues. Manage pharmacovigilance for assigned projects and oversee ongoing safety reviews
Später ansehen16.06.24 | Vollzeit | München | JobLeads GmbH | 100.000 € - 125.000 € Experience in pharmaceutical industry and/or clinical research organization, including clinical study/project management/clinical trial management. - Experience of managing clinical programs through phase 1-4. - Metabolic or obesity trial experience - Thorough knowledge of FDA and ICH GCP guidelines
Später ansehen14.06.24 | Vollzeit | München | JobLeads GmbH | 125.000 € - 150.000 € Cycle. He/she is a peer scientific expert who communicates accurate and applicable scientific and medical information to Healthcare Practitioners (HCPs) within a geographic area. In addition, the MSL manages and maintains collegial and professional relationships with HCPs and identifies and facilitates
Später ansehen14.06.24 | Vollzeit | München | JobLeads GmbH | 100.000 € - 125.000 € clinical trials. Some of your daily tasks will include - Overseeing the planning and management of clinical trials, including selection and supervision of CROs. - Contributing to clinical development plans and study protocols from the operations perspective. - Being a key member of a cross-functional
Später ansehen14.06.24 | Vollzeit | Gräfelfing | JobLeads GmbH | 125.000 € - 150.000 € Review study data, making strategic recommendations to meet project goals. - Develop and refine clinical protocols, overseeing medical monitoring and ongoing medical data review, including protocol exemptions, violations, and eligibility issues. - Manage pharmacovigilance for assigned projects
Später ansehen13.06.24 | Vollzeit | München | JobLeads GmbH | 125.000 € - 150.000 € clinical development plans, clinical trial protocols, and statistical analysis plans in collaboration with our biopharma partners. - Leads and oversees statistical deliverables including but not limited to execution of statistical analyses, interim safety and efficacy reports, clinical study reports
Später ansehen13.06.24 | Vollzeit | Gräfelfing | Immunic AGStrategic recommendations to meet project goals. Develop and refine clinical protocols, overseeing medical monitoring and ongoing medical data review, including protocol exemptions, violations, and eligibility issues. Manage pharmacovigilance for assigned projects and oversee ongoing safety reviews
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