Mark Baugh Email & Phone Number

Stirling, Scotland, United Kingdom

Stirling

Livingston

Establish and monitor laboratory quality and technical systems including assay quality control, proficiency testing review, the scientific database and global laboratory meetings. Collaborate with the assay development laboratory, regional production laboratories, scientific review, data management, vendors and laboratory management.· Plan, schedule, conduct, report and close global assay quality control reviews, monitor regional and/or global trends, implement corrective actions when… Show more Establish and monitor laboratory quality and technical systems including assay quality control, proficiency testing review, the scientific database and global laboratory meetings. Collaborate with the assay development laboratory, regional production laboratories, scientific review, data management, vendors and laboratory management.· Plan, schedule, conduct, report and close global assay quality control reviews, monitor regional and/or global trends, implement corrective actions when needed to establish or restore acceptable global performance· Plan, schedule, conduct, report and close the global review of regional laboratory investigations performed for proficiency testing failures and interacts with laboratory management regarding regional laboratory compliance with process improvements· Ensure the Scientific Database and the test code system are updated with accurate information.· Ensure the global inventory of harmonized reagents, calibrators and quality control materials is maintained· Write sponsor communications regarding technical assay updates impacting active protocols.· Participate in laboratory management discussions with vendors regarding technical assay issues, global pricing and global reagent inventory delivery· Provide training to Global Harmonization team and regional laboratory teams, as needed· Facilitate global technical meetings Show less

Livingston

• Primary contact for Sponsors throughout duration of the clinical trial. • Coordinating project initiation in conjunction with Set-Up Management team and Sponsor. • Responsible for monitoring adherence to protocol requirements and protocol-specific timelines.• Ensuring continuity throughout the life of the project and coordinating study closure.

Glasgow, United Kingdom

• Determination of synthetic lethality and drug synergism using in vitro high content screening, assays of cell viability and flow cytometry.• Coordination of screening at collaborative sites in UK

• Senior Pharmacologist of a Lead Optimisation Project with approximately 20 members, cross-site with The Netherlands.• Member of new therapeutic targets assessment team. • Manager of in-house in vivo data software• Health & Safety representative • Line management & student supervision• In vitro and in vivo assay design, SOP generation and problem solving.• PRINCE2 project management & GLP

Investigation into the role of monocytes in vascular disease in type 2 diabetes: • Comparison of cell activity using migration assays, cell differentiation.• The role of nuclear receptors in monocyte/macrophage biology.• Analysis of protease activity using ELISA, immunoblotting, substrate assays.• Analysis of lipoprotein modification and protease levels in patient groups. • Supervision of undergraduate research projects and research assistants

Pgde, Primary Education

Phd, Medical Research

A study of matrix metalloproteinases in inflammatory bowel disease (IBD): • Effects of collagen and cytokines on fibroblast morphology &.

Bsc(Hons) 2.1, Biology

Education record