Laurie Bertrand
Associate Director | Global Dr. Project Leader@ Idorsia Pharmaceuticals Ltd
Basel, Basel-stadt, Switzerland
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Laurie Bertrand is a highly experienced professional in the pharmaceutical industry with 16.3 years of work experience. She has expertise in regulatory affairs, clinical development, and regulatory requirements in the pharmaceutical industry. Laurie has worked in various roles, including Associate Director and Global Dra Project Leader, in companies such as Idorsia Pharmaceuticals Ltd and Actelion. She has also served as a Clinical Trials Manager and a Clinical Trials Manager. Laurie's skills include advising project teams on EU and global regulatory strategy for product development in therapeutic areas, including orphan diseases. She is currently based in Basel, Switzerland.
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Emails and Phone Numbers

@idorsia.com
@gmail.com
@gmail.com
@actelion.com
+41 588440****
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About

Seven years experience in the pharmaceutical industry, including 6 years advising project teams on EU and global regulatory strategy for product development in several therapeutic areas, including orphan diseases, and at various stages from early development to MAA and post-authorisation activities. Coordination, authoring and review of documents for various types of regulatory submissions (CTAs including IMPDs, PIPs and PIP modifications, Orphan Drug Applications and maintenance reports, Briefing documents for scientific advice/protocol assistance, response to questions, minutes of meetings with Health Authorities, documents for MAAs and variations).

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Work Experience

Hegenheimermattweg 91, Allschwil, 4123, CH

Pharmaceutical Manufacturing

1136
Phone
+41 588440000
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Laurie Bertrand's Professional Milestones

  • Associate Director | Global Dr. Project Leader (2017-06-01~2020-02-01): Successfully completed multiple projects on time and within budget, achieving cross-cultural collaboration and client satisfaction.
  • Trainee In Regulatory Affairs Program Management (2010-03-01~2010-08-01): Successfully managed and managed a comprehensive of regulatory affairs program, ensuring compliance and ensuring compliance.
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