Tatjana Alberg

Gehägestr. 46a
D-30655 Hannover
Phone: +49 511 692030
Fax: +49 511 692074
Mobile: +49 172 436 9773

tatjana.alberg@cra-freelance.net
www.proclintas.de

Born in Hannover, Germany, 1969

Professional experience

  • National and international clinical trials and post marketing studies
  • Conduct Pre-study-, Initiation-, Interim- and Closeout monitoring visits in Phase I-IV Trials.
  • Manage trip reports, query resolutions and payment instructions
  • Provide support and timely follow-up for audit + quality assurance activities
  • Web based data capture (eTrials)
  • Co-Monitoringvisits with new colleagues
  • Training for investigational staff (ICH/GCP, AMG, SAE/AE)
  • Instructing of sites in the use and maintenance of IVRS
  • Feasibility Checks and site selection
  • Indications: oncology, nephrology, cns and pain

Employments

  • Since 10/2007 self employed, own company “proclintas – professional clinical trial assistance”
  • 01/2005 – 09/2007 Ortho Biotech, Division of Janssen-Cilag GmbH Neuss, Clinical Research Associate (homebased), Oncology & nephrology
  • 11/2003 – 12/2004 AstraZeneca GmbH Wedel, Medical Project Manager (homebased), CNS
  • 01/2003 – 10/2003 AstraZeneca GmbH Wedel, Clinic medical representative (homebased), CNS
  • 01/1998 – 12/2002 Pharmacia GmbH Erlangen, Medical representative (homebased), general medicine

Education / Qualification

  • since 01/2005 continuous QUALIFICATIONS in processes of clinical research, monitoring and data management, communication, medicine, quality assurance – for details see also training record.
  • 1990-1997 Studies of Biology, Universities Frankfurt/M. and Hannover, final certificate: biological diploma
  • since 01/2005 continuous QUALIFICATIONS in processes of clinical research, monitoring and data management, communication, medicine, quality assurance – for details see also training record.
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