Experience

Debiopharm

• Switzerland
• Pharmaceutical Manufacturing
• 300 - 400 Employee

• Senior Medical Writer

  • Jan 2016 - Jun 2019

• Clinical Research and Communications consultant

  • Jun 2005 - Dec 2015

  Document writing for clinical research (protocols, informed consents, study reports, investigator drug brochures, etc.) and the scientific community (scientific articles and presentations; poster design and writing).



EMD Serono, Inc.

• Pharmaceutical Manufacturing
• 700 & Above Employee

• Clinical Research and Communications consultant

  • Sep 1997 - Apr 2005

  - Corporate Medical Communication Services (writing medical documents, handling medical FAQs, developing and providing training on medical inquiries database) - Corporate Marketing Communications & Public Relations (developing press kits, writing media releases, company statements, and FAQ sheets) - Corporate Medical Affairs (writing clinical research documents, reviewing case report forms, data validation plans, and data queries, and following up study centres) - Corporate World-wide… Show more - Corporate Medical Communication Services (writing medical documents, handling medical FAQs, developing and providing training on medical inquiries database) - Corporate Marketing Communications & Public Relations (developing press kits, writing media releases, company statements, and FAQ sheets) - Corporate Medical Affairs (writing clinical research documents, reviewing case report forms, data validation plans, and data queries, and following up study centres) - Corporate World-wide Drug Safety (writing core safety data sheets, developing document database, assessing clinical cases) - Corporate Biometrics (writing and reviewing data validation plans, case report forms, and data queries) Show less - Corporate Medical Communication Services (writing medical documents, handling medical FAQs, developing and providing training on medical inquiries database) - Corporate Marketing Communications & Public Relations (developing press kits, writing media releases, company statements, and FAQ sheets) - Corporate Medical Affairs (writing clinical research documents, reviewing case report forms, data validation plans, and data queries, and following up study centres) - Corporate World-wide… Show more - Corporate Medical Communication Services (writing medical documents, handling medical FAQs, developing and providing training on medical inquiries database) - Corporate Marketing Communications & Public Relations (developing press kits, writing media releases, company statements, and FAQ sheets) - Corporate Medical Affairs (writing clinical research documents, reviewing case report forms, data validation plans, and data queries, and following up study centres) - Corporate World-wide Drug Safety (writing core safety data sheets, developing document database, assessing clinical cases) - Corporate Biometrics (writing and reviewing data validation plans, case report forms, and data queries) Show less



d-TARGET S.à.r.l.

• Yverdon, Switzerland

• Clinical research consultant

  • Oct 2000 - Oct 2002

  Report, protocol, and guideline generation; case report form design for various projects; management and review of adverse events (Device Safety Officer) for all ongoing study projects; input into study and data management. Report, protocol, and guideline generation; case report form design for various projects; management and review of adverse events (Device Safety Officer) for all ongoing study projects; input into study and data management.



EMD Serono, Inc.

• Pharmaceutical Manufacturing
• 700 & Above Employee

• Director, Scientific and Medical Communications

  • Nov 1993 - Apr 1997

  Set up a medical information and publication department for the Group. - Established central library - Organised scientific communications process - Created scientific information bulletin - Launched Internet, CD-ROM network, developed literature database - Produced books and brochures for institutional or marketing use - Selected medical communication agencies and writers

• Manager, European Clinical Research Associates

  • Jan 1991 - Oct 1993

  Established and managed a new department of corporate clinical research associates comprising 9 home-based study monitors in various European countries reporting to Geneva headquarters. Ensured quality monitoring of clinical trials carried out for drug registration purposes as per international clinical research standards in more than 100 study centres.