Craig Oswald Email & Phone Number

Responsible for the management of safety activities for global Phase I-III clinical trials from start-up through to closeout, with a focus in oncology, rare and infectious disease studies. Also line management, recruitment, business development activities, and safety proposals and budgets.Achievements:Recruitment and development of EU safety teamRegulatory submissions oversightBusiness development and strategic planningProcess improvement and SOP review

Edinburgh, Scotland, United Kingdom

Stirling

Management of clinical safety studies as well as the line management of project assistants and clinical study coordinators. Regular client interactions, working to successfully deliver safety services on their studies.Achievements:Management of support PA group activitiesAuthentic and empathic line managementMentoring of safety specialists into safety manager roles

Edinburgh

Responsible for coordinating serious adverse event review, tracking and reporting activities. Effectively interfacing with project teams, client companies and investigators regarding SAE activities on large Phase III clinical trials. Leading PV studies and overseeing study budgets. Regular client interactionsAchievements:SAE reporting KPIs to identify data quality issues at specific study sites. Deputised for line manager

Responsible for coordinating serious adverse event review, tracking and reporting activities. Maintaining knowledge and understanding of PPD SOPS; current ICH GCP/Local guidelines regarding clinical trials, regulatory compounds and effectively interfacing with project teams, client companies and investigators regarding SAE activities. Leading studies and overseeing study budgets. Regular client interactions.

See above description

Edinburgh

Line manager for a team of junior staff as well as being a responsible scientist performing cardiovascular safety studies to GLP regulations. This also included data analysis and reporting of results. I was also an application manager for departmental computer systems. In addition I was also in charge of my groups purchasing and supplies facility. Previous responsibilities included performing the role of departmental health and safety representative and manual handling assessor.

Edinburgh

Responsible for conducting models of disease states as part of the drug discovery process as well as performing ligand binding experiments and histological processing.