Anne Watrin
About Anne Watrin
Anne Watrin serves as the Director Clinical at ONWARD, where she has worked since 2023, managing a team of five and coordinating clinical studies. With a background in biochemistry and regulatory affairs, she has held various roles in clinical program management and regulatory compliance.
Work at Onward
Anne Watrin serves as the Director Clinical at ONWARD since 2023. In this role, she manages a team of five individuals and coordinates ongoing clinical studies. Her responsibilities include ensuring effective collaboration between internal and external teams. She also develops essential documentation for international, multi-center clinical studies, such as Clinical Investigation Plans (CIP), Investigator's Brochure (IB), Informed Consent Forms (ICF), and Case Report Forms (CRF). Previously, she held the position of Clinical Program Manager at ONWARD from 2020 to 2023.
Education and Expertise
Anne Watrin has an extensive educational background in the life sciences. She studied Biochimie, Biologie cellulaire et Physiologie at Université de Franche-Comté, where she earned her Licence from 2010 to 2013. She further pursued her studies at Université Laval, achieving a Baccalauréat in Biochimie from 2012 to 2013. Additionally, she obtained a Diplôme d'ingénieur in Génie biomédical from ISIFC, completing her studies from 2013 to 2016. Since 2015, she has been studying crisis management at WAR ROOM.
Background
Anne Watrin began her career in the clinical field with a role as Stage Hospitalier at EFS in Bourgogne Franche-Comté in 2015. She later worked as a Regulatory Affairs Intern at GSK in Nyon for four months in 2016. From 2014 to 2015, she served as Ingénieur Affaires Réglementaires, Propriétés Intelectuelles et Valorisation at Biotika® in Besançon. Her diverse experiences in clinical management and regulatory affairs have contributed to her current expertise in clinical study coordination.
Clinical Study Coordination
In her current role at ONWARD, Anne Watrin acts as the project coordinator for ongoing clinical studies. She ensures that there is effective collaboration between various internal and external teams involved in these studies. Her responsibilities also include interacting with regulatory authorities for the initiation of clinical studies, ongoing reporting, and submissions of clinical data for market approval. This role highlights her capability in managing complex clinical projects and regulatory compliance.