Laura Crawford
About Laura Crawford
Laura Crawford is the Associate Director of Trial Supplies Management at Bristol Myers Squibb in Hillingdon, England, with over a decade of experience in the pharmaceutical industry.
Company
Laura Crawford is currently employed at Bristol Myers Squibb, a globally recognized pharmaceutical company. She serves as the Associate Director of Trial Supplies Management. This role is based in Hillingdon, England, United Kingdom. Bristol Myers Squibb is known for its focus on developing innovative therapies across various therapeutic areas.
Title
Laura Crawford holds the title of Associate Director, Trial Supplies Management at Bristol Myers Squibb. In this capacity, she oversees the management of trial supplies, ensuring the timely and efficient delivery of materials necessary for clinical trials. Her role is critical to the successful execution and management of clinical studies.
Previous Roles at Celgene
Before joining Bristol Myers Squibb, Laura Crawford worked at Celgene. She held the position of Senior Manager, Forecasting and Planning, from 2017 to 2020, where she managed forecasting and planning activities. Additionally, she served as a Senior Strategic Planner at Celgene, contributing to the company's strategic initiatives. During her 3-year tenure at Celgene, she developed significant expertise in forecasting, planning, and strategic management.
Experience and Expertise in Pharmaceuticals
Laura Crawford has accumulated over a decade of experience in the pharmaceutical industry. Her specialization lies in trial supplies management and strategic planning. She is well-versed in the complexities of managing clinical trial supplies and has a strong background in forecasting and planning, which are crucial aspects of pharmaceutical operations.
Career at Bristol Myers Squibb
Since joining Bristol Myers Squibb in November 2020, Laura Crawford has been instrumental in managing trial supplies as the Associate Director, Trial Supplies Management. Her extensive experience in the pharmaceutical industry enables her to effectively oversee supply chain activities related to clinical trials, ensuring operational efficiency and compliance.