20.04.24 | Vollzeit | Innsbruck | MED-EL Medical ElectronicsProcedures - Oversee study activities, manage timelines, coordinate monitors, and work with clinical evaluation managers, data managers, and statisticians - Manage study documentation and regulatory submissions, maintaining accurate and complete documentation, including protocols, informed consents, case
Später ansehen24.04.24 | Vollzeit | Wien | JobLeads GmbH | € 100.000 - € 125.000 Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest
Später ansehen19.04.24 | Vollzeit | Wien | JobLeads GmbH | € 100.000 - € 125.000 Workplace Recognized for our culture and way of working, we’re one of only 17 companies to receive Top Global Employer status for 2024. Work-Life Work-Life Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family. Empowerment Empowerment Through
Später ansehen17.03.24 | Vollzeit | Wien | JobLeads GmbH | € 100.000 - € 125.000 As required - Develop, implement and supervise company-sponsored non-interventional studies in alignment with legal and compliance requirements and internal SOPs/Policies; manages publication of study results. - Manage investigator-initiated studies in alignment with legal and compliance requirements (AMG
Später ansehen25.04.24 | Vollzeit, Teilzeit | Tulln an der Donau | biotechjobs.atInternational clinical trials • Manage clinical trial preparation and progress, establish and s upervise relationships with investigators • Counsel and guide Clinical Research Associates (CRAs) and Contract Rese arch Organizations (CROs) • Review trial related documents/reports, plan study budget, timelines
Später ansehen12.01.24 | Vollzeit | JobLeads GmbH | € 125.000 - € 150.000 Will focus on clinical development in the area of dermatology in phases II-III of clinical trials. Responsibilities - Provide internal and external partners with expertise in dermatology area - Contribute to protocol and other study documents creation - Cooperate with PV to ensure that all relevant plans
Später ansehen12.01.24 | Vollzeit | JobLeads GmbH | € 125.000 - € 150.000 Of clinical trials. In this position you will - Provide internal and external partners with expertise in pulmonology area - Contribute to protocol and other study documents creation - Cooperate with Drug Safety to ensure that all relevant plans are in place to properly assess safety - Act as medical reviewer
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