Regional Clinical Trial Manager (m/f): The Regional Clinical Development Department located in Vienna manages and coordinates international clinical trials including Austria, Switzerland, Israel and Central and Eastern European countries. We are currently seeking a motivated professional Regional Clinical Trial Manager.
Job Profile
- Prepare and coordinate international clinical trials in the Region described above
- Manage clinical trial preparation and progress
- Establish and supervise relationships with investigators
- Counsel and guide Clinical Research Associates (CRAs) and Contract Research Organizations (CROs)
- Review trial related documents and reports
- Plan study budget, timelines and capacities
- Ensure timely submission to Ethic Committees and Competent Authorities
- Train and lead the trial coordinators and CRAs
- Supervise monitoring activities and perform Co-Monitoring Visits
- Organize and conduct investigator meetings
- Work in virtual teams
Boehringer Ingelheim offers competitive compensation. This position is remunerated according to qualification in regard to full-time employment with an annual total target of not less than € 56,737.– gross, depending on experience higher remuneration is possible. Moreover, we provide attractive social benefits to our employees.
Requirements
- MD qualification is preferred; qualification in biological/natural science will be considered
- Prior experience in pharmaceutical industry for at least 3-5 years as on-site monitor (CRA) or clinical trial manager in the therapeutic field of respiratory and/or immunology diseases preferred
- Good knowledge of international and national/regional guidelines and regulatory topics
- Experience in project/trial management is an asset
- Fluency in written and spoken English
- Leadership potential; excellent analytical, organizational and decision making skills
- Innovative and takes initiative – you are ready to challenge and actively pursue novel ways
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Job ID:153473
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Career Level:Experienced
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Location:
Austria
(Vienna)
Vienna -
Function:Medicine / Regulatory Affairs
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Schedule:Full-Time
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