Clinical Reporting and Documentation Specialist
Zealand Pharma
10 years experience within clinical documentation for regulatory submission and clinical trial transparency, with a strong focus on the collaboration and strategy between Clinical and Regulatory groups, in large and mid-size pharma. Subject matter expert and implementation Project Manager for the EU Clinical Trial Regulation implemenation project at Zeland Pharma A/S.
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Monday, September 12, 2022
2:00 PM – 3:00 PM MST