BioPharma Services
Allan Ligon has a diverse work experience spanning several companies and roles. Allan is currently working as the Director of Corporate IT at Think Research since November 2021. Prior to this, Allan served as the Director of Information Technology at BioPharma Services Inc. for over 3 years, starting in January 2020. Before that, they held the position of IT Manager at the same company for 7 years. Allan's earlier experience includes working as a Consultant - IT / Customer Support Services and later as the Business Head - IT / Customer Support Services at SMS Global Technologies Inc. for a total of 23 years. Allan started at SMS Global Technologies Inc. in July 1998 and left in July 2021. Allan's work history also includes a role as an IT Administrator at VLS Logistics Services from June 2011 to June 2013.
Allan Ligon began their education in 1993 at AMA University, where they pursued a Bachelor of Science in Computer Engineering, which they completed in 1997. Later, in 2010, they attended the Citi College of Canadian Careers to study Network Engineering in the field of Information Technology.
In terms of additional certifications, Allan Ligon obtained the CompTIA A+ certification from CompTIA in December 2010. Allan then went on to earn multiple certifications from Microsoft, including Microsoft Certified Technology Specialist in January 2011, Microsoft Certified Professional in February 2011, and Microsoft Certified IT Professional Enterprise Administrator in April 2011.
Recently, in August 2021, Allan Ligon obtained the ITIL Foundation Level v4 certification from AXELOS Global Best Practice.
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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.