BioPharma Services
Anna Taylor has a long and successful career in the pharmaceutical industry. Anna started in 2003 as a Senior Project Manager at Cetero Research before moving to Bio Pharma Services, Inc. in 2007. At Bio Pharma Services, Inc., they held multiple roles including Manager of Business Development and Senior Project Manager. In 2011, they became the Director of Business Development at the same company. Most recently, Anna has been serving as the Executive Vice President of Business Development at BioPharma Services Inc. since 2015.
Anna Taylor attended Laurentian University/Université Laurentienne to pursue a Bachelor of Science degree in Human Biology. The duration of their enrollment and the completion status of their degree are not provided.
BioPharma Services
BioPharma Services Inc. is a full-service Contract Research Organization (CRO) specializing in Phase I/IIa, Bioequivalence, Human Abuse Liability, PET Imaging and Psychedelic Studies. With over 17 years of industry experience, and a primary research facility in Toronto, Canada, our team of experts are dedicated to delivering superior quality service and reliable research results. BioPharma Services offers in-house, GLP/GCP preclinical and clinical bioanalytical services, featuring LC-MS/MS technology at our Toronto facility. We prioritize ethical subject recruitment and comply with all major international regulatory bodies, including the FDA, Health Canada, and ANVISA. We have been successfully inspected by all major regulatory bodies, and are dedicated to building and maintaining long-lasting relationships with our Global clients through superior quality service, timely and reliable research results. Highlights of our experience: → State-of-the-art Clinical facility in Canada with over 150 bed capacity → 99% enrolment for all Phase I studies with a 95% completion rate → Timely study start up: 30 Day CTA, Weekly IRB/Ethics review → 20,000+ active subject database of patients, special populations & healthy volunteers → Full service capabilities: Regulatory, Scientific and Medical Affairs, Comprehensive Project Management, Data Management, Biostatistical Analysis with CDISC data standards (SDTM and ADaM datasets), Medical Writing and more.