Maureen Drouin
About Maureen Drouin
Maureen Drouin is the Director, Pharmacovigilance Scientist at Bristol-Myers Squibb, with over 20 years of experience in the pharmaceuticals industry.
Company
Maureen Drouin currently works at Bristol-Myers Squibb as the Director, Pharmacovigilance Scientist. Prior to this role, she served as a Senior Pharmacovigilance Scientist within the same company. Bristol-Myers Squibb is a global biopharmaceutical company known for focusing on the discovery, development, and delivery of innovative medicines. Maureen's long tenure at this company highlights her deep-rooted experience and commitment to advancing pharmaceutical safety and efficacy.
Title
Maureen Drouin holds the title of Director, Pharmacovigilance Scientist at Bristol-Myers Squibb. This position underscores her leadership role and her extensive expertise in the field of Pharmacovigilance, ensuring the safety and effectiveness of pharmaceutical products.
Education and Expertise
Maureen Drouin earned her Bachelor's degree in Registered Nursing/Registered Nurse from Southern Connecticut State University. Her educational background provides a strong foundation in the medical field, complementing her extensive experience in Pharmacovigilance activities. Specific areas of expertise include PBRER/DSUR preparation, signal detection, responding to ad hoc queries, Vendor Management, Oncology, Clinical Trials, and Medical Writing. Her combined educational and experiential background makes her a versatile and knowledgeable professional in pharmaceuticals.
Professional Background
Maureen Drouin has more than 20 years of experience in the pharmaceuticals industry, starting her current role as Director, Pharmacovigilance Scientist in July 2002. Her career trajectory has been largely centered on Pharmacovigilance, with a notable history of managing and leading critical safety operations. She has significant experience conducted in various Pharmacovigilance roles, which have solidified her reputation in the industry.
Specialties and Research
With a strong research background in Pharmacovigilance, Maureen Drouin specializes in the preparation of PBRER/DSUR, conducting signal detection, and managing ad hoc queries. Her expertise spans Vendor Management, Oncology, Clinical Trials, and Medical Writing. These specialized skills are essential in ensuring the safety and regulatory compliance of pharmaceutical products. Maureen’s deep knowledge and skills make her a key contributor to her field.