Olive Watson Coleman

Olive Watson Coleman

Senior Clinical Compliance Auditor @ Bristol Myers Squibb

About Olive Watson Coleman

Olive Watson Coleman is a Senior Clinical Compliance Auditor at Bristol-Myers Squibb in New York, with over 23 years of experience in various roles at the company.

Title: Senior Clinical Compliance Auditor

Olive Watson Coleman is currently a Senior Clinical Compliance Auditor at Bristol-Myers Squibb. She has been in this role for over 12 years, contributing to the integrity and compliance of clinical sites. Her responsibilities include ensuring that clinical trials are conducted in adherence to regulatory requirements and company policies, safeguarding the quality and accuracy of clinical data.

Company: Bristol-Myers Squibb

Olive Watson Coleman has worked at Bristol-Myers Squibb for an extensive period, accumulating over 23 years of experience in various roles. She has contributed significantly to the company's clinical operations, transitioning through numerous positions including Clinical Site Manager, Senior Clinical Site Manager, and now, Senior Clinical Compliance Auditor. Her longstanding tenure exemplifies her dedication and expertise in the pharmaceutical industry.

Education and Expertise: Southern Connecticut State University

Olive Watson Coleman completed her academic training at Southern Connecticut State University, earning a Bachelor of Science in Nursing and a Master of Public Health. Her education from 1987 to 1995 laid a strong foundation for her career in clinical compliance and site management. This blend of nursing and public health education equips her with a comprehensive understanding of clinical operations and regulatory compliance.

Background: Clinical Site Manager at Bristol-Myers Squibb

Before becoming a Senior Clinical Compliance Auditor, Olive Watson Coleman served as a Clinical Site Manager and then as a Senior Clinical Site Manager at Bristol-Myers Squibb. She held the Clinical Site Manager role from 2000 to 2006 and advanced to Senior Clinical Site Manager from 2006 to 2011. These roles involved overseeing clinical trial sites, ensuring regulatory compliance, and managing site operations effectively.

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