Tanja Baumann
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Fähigkeiten und Kenntnisse
Werdegang
Berufserfahrung von Tanja Baumann
- Current 5 years and 3 months, since Mar 2021
Sales & Operations
Satellites of Art GmbH
- 2 years and 2 months, Aug 2011 - Sep 2013
Senior Program Manager, Project Management
Vifor Pharma Ltd
- 1 year and 10 months, Oct 2009 - Jul 2011
Head Clinical Project Management
Auron Healthcare AG
- 2 years and 2 months, Aug 2007 - Sep 2009
Development Project Leader
Arpida
Provide strategic input to Nonclinical and Clinical Development programs and take the lead to ensure successful initiation and conduct of clinical and non-clinical studies. Overall responsibility for the assigned project and the associated studies and other related activities, involved into decisions concerning study strategy, timelines, overall logistics, scientific and medical aspects as well as budget issues.
- 2 years and 10 months, Sep 2002 - Jun 2005
Senior Project Manager / Company Director CH
TEAMworks Clinical Solutions AG
Responsible for the management of over 30 clinical research projects using EDC deployed on a global basis. The studies covered a wide range of therapeutic areas including diabetes, asthma, oncology, coronary heart disease, transplant and dermatology. In addition, in the role of Company Director, managed the financial and administrative setup and maintenance of the Swiss branch of the TEAMworks company
- 2 years and 3 months, Jun 2000 - Aug 2002
Project Manager
TEAMworks Clinical Solutions AG
Management of customer clinical research projects using electronic data capture tool. Design of eCRFs according to protocol and customer requirements – including creation of specification documents, verification of eCRF and liaison with customer project personnel to ensure all deliverables were met on time and to their expectations. Training of external personnel (sponsor and site staff) in the use of the EDC tool on site and at investigator meetings and creation of training materials
- 1 year and 8 months, Sep 1998 - Apr 2000
Clinical Trials Coordinator (CTC)
The R.W. Johnson Pharmaceutical Research Institute
Responsible for the planning, organization, supervision (monitoring), administration and management of Proof of Principle studies, mainly in the therapeutic areas of cardiovascular medicine. The investigative centers responsible for were situated in Switzerland, Germany, the Netherlands and the United Kingdom.
- 2 years and 1 month, Aug 1996 - Aug 1998
Clinical Research Coordinator (CRC)
The R.W.Johnson Pharmaceutical Research Institute
Coordination of clinical database review, reconciliation and finalization activities. Participation in overseeing all clinical data management tasks per study from protocol review, CRF design, database design, edit checks specification, validation, testing and database release to monitoring query processing and resolution, including quality control procedures and data base lock. Acting as a liaison between clinical operations and external database management CRO.
Ausbildung von Tanja Baumann
- 5 years and 1 month, Sep 1990 - Sep 1995
Biologie
ETH Zürich
Verhaltensbiologie
Sprachen
German
C2 (Verhandlungssicher / Muttersprachlich)
English
C1 (Fließend)
French
B1-B2 (Gute Kenntnisse)
Danish
C1 (Fließend)
Italian
A1-A2 (Grundkenntnisse)
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