Denise Naylor
About Denise Naylor
Denise Naylor is a Protocol Data Manager at Bristol-Myers Squibb, responsible for ensuring clarity and consistency in data collection and maintaining Global Standards.
Company
Denise Naylor is employed at Bristol-Myers Squibb. She has been an integral part of the company since July 1989. Bristol-Myers Squibb, a global biopharmaceutical company, focuses on discovering, developing, and delivering innovative medicines for patients with serious diseases. Denise’s long tenure at the company highlights her significant experience and dedication to her role.
Title
Denise Naylor holds the position of Protocol Data Manager at Bristol-Myers Squibb. In this role, she is responsible for a range of critical tasks that support the company’s clinical trials and data integrity.
Roles and Responsibilities
In her role as Protocol Data Manager, Denise Naylor reviews draft protocols to ensure clarity and consistency in data collection. She identifies new data requirements and spearheads the creation of new modules for data entry or loading. Denise maintains and promotes established Global Standards, creates timelines for study start-up activities, and facilitates meetings with project teams to document vendor selection and tracking requirements. She also creates Case Report Forms (CRFs) for studies, selects and tests derivations, and reviews and approves database packages based on final CRFs for production.
Expertise in Clinical Trials
Denise Naylor's expertise is central to the clinical trial process at Bristol-Myers Squibb. She plays a vital role in ensuring that all protocols are clear and consistent for data collection. Her work in identifying new data requirements and developing modules ensures that the clinical trials are equipped with the necessary tools to collect accurate data. Denise's involvement in meetings with project teams, and her responsibility in tracking requirements for protocol-specified assessments, further emphasizes her intricate understanding of the clinical trial landscape.