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Clinical Project Manager - Vienna
The successful candidate is responsible for planning, managing and reporting of international clinical studies on plasma-derived products. The scope of duties includes site selection, study conduct and data resolution as well as reviewing protocols and regulatory documents.
Requirements:
- Significant medical background
- Minimum of 5 years clinical research experience in a CRO, pharmaceutical or biotechnology company
- Experience of multi-centre/multi-national clinical studies and/or direct monitoring
- Strong organisational, presentation, documentation and interpersonal skills
- Proven experience in all clinical aspects of a trial with a strong knowledge of applicable regulations and accepted practices
- Good clinical knowledge with an understanding of medical terminology
- Advanced computer skills (Internet, Microsoft Office)
- Excellent English (written and spoken) and communication skills
- Willingness to travel
To Apply:
If you feel qualified please send your application including a CV with a detailed description of your relevant experience:
Octapharma Pharmazeutika Produktionsges.m.b.H.
Oberlaaer Straße 235
1100 Wien
Tel: 01/610 32 –311, Fr. Mag.(FH) Romana Bogner
email: jobs@octapharma.at
Octapharma is an Equal Opportunities Employer.
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