Frederique Cousin
About Frederique Cousin
Frederique Cousin is a Senior Study Start-Up Specialist at Bristol Myers Squibb, with over 18 years of experience in clinical research and extensive expertise in managing international clinical trials.
Current Role at Bristol Myers Squibb
Frederique Cousin currently holds the position of Senior Study Start-Up Specialist at Bristol Myers Squibb, where she works through Syneos Health. She is based in Rueil-Malmaison, Île-de-France, France. In this role, she is responsible for initiating clinical studies and facilitating study start-up activities, ensuring compliance with regulatory requirements.
Previous Experience as Senior Study Start-Up Specialist
Before taking on her current role, Cousin worked as a Site Trial Manager at Bristol Myers Squibb for 10 months in 2019, also through Syneos Health. Her role entailed managing site trials and ensuring that trial processes were executed efficiently in compliance with regulatory standards.
Experience at Roche and Servier
Frederique Cousin served as a Country Study Manager at Roche from 2018 to 2019, working through Hays Pharma in Région de Boulogne-Billancourt, France. Prior to that, she was a Clinical Operation Project Manager at Servier from 2017 to 2018, outsourced through Kelly OCG, where she managed clinical operations in the Région de Paris, France.
Role at MSD
Cousin's experience also includes working at MSD as a Regulatory Clinical Operations Manager between 2015 and 2017 in Courbevoie. She was responsible for overseeing regulatory aspects and clinical operations. Before that, she worked at MSD as a Regulatory Associate (Contractor) in 2015 for 7 months.
Educational Background
Frederique Cousin has a diverse educational background. She studied Eléments de santé au travail pour les ingénieurs et managers at Conservatoire National des Arts et Métiers, earned a Certificat Clinical Research Associate from Clinact, and achieved a Postgraduate degree in Biochemistry from the University Chemistry at Montpellier. Additionally, she holds a Master of Chemistry Biology from the University of Sciences at Nantes.
Clinical Research Expertise
With over 18 years of experience in Clinical Research, Frederique Cousin specializes in the management of international clinical trials including Phase III, IIIb, IV, late phase, observational, and epidemiology studies. She possesses expertise in regulatory requirements and GCP-ICH knowledge, ensuring compliance in clinical trials.