Appointment as Director of Revival Radio - the company that holds the broadcast license and manages both 93 FM and 100.8 Revival FM. Company and position registered with Companies House (UK).

• Planning and management of clinical studies conducted by Global Development through the leadership of the cross-functional Clinical Study Team (CST)• Contributing to study-level risk assessments • Leading and continually review risk mitigation activities to ensure study delivery to plan • Identifying and resolving issues at a global level • Reporting study progress at appropriate forums and to management • Collaborating with Regional CTM to ensure country level study… Show more • Planning and management of clinical studies conducted by Global Development through the leadership of the cross-functional Clinical Study Team (CST)• Contributing to study-level risk assessments • Leading and continually review risk mitigation activities to ensure study delivery to plan • Identifying and resolving issues at a global level • Reporting study progress at appropriate forums and to management • Collaborating with Regional CTM to ensure country level study delivery aligned with global delivery plans • Overseeing global insourcing/outsourcing partner deliverables to the required standards • Managing study-level budget and timelines • Partnering with Tech Services, Supplier Governance and Electronic Trial Operations - to ensure vendor set-up, conduct and quality oversight of deliverables • Leading global study-level documentation and required tool and systems set-up • Leading development and implementation of global Drug Supply Plan • Ensuring implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines Show less

Providing leadership to the PAREXEL and Client teams by combining a depth of clinical research experience with insight in to client pressures. Developing the right solution for the client. Making effective decisions independently based on demonstrated in-depth, business understanding .Demonstrating the required knowledge and experience to confidently recommend a course of action where client intervention is required. Providing overall leadership of large and complex clinical… Show more Providing leadership to the PAREXEL and Client teams by combining a depth of clinical research experience with insight in to client pressures. Developing the right solution for the client. Making effective decisions independently based on demonstrated in-depth, business understanding .Demonstrating the required knowledge and experience to confidently recommend a course of action where client intervention is required. Providing overall leadership of large and complex clinical trials or clinical programs and to project teams to achieve operational excellence. Leading the delivery of projects/programs on time, within budget and to the highest quality, compliant with ICH-GCP and exceeding client expectations. Responsible for the profitability of a project(s) or program(s) client satisfaction. Acting as a client focused role model and/or mentor for the team. Show less

Providing oversight of clinical projects. Activities include:Ensuring implementation of the scope of work, handover from Business Development to Clinical Project Manager, including Clinical Trial Management System (CTMS) set-up.Overseeing the implementation of CTMS in the Clinical Department including training requirements and project implementation,Ensuring development and implementation of project plans, communication plans, Training plans, TMF plans and other plans as… Show more Providing oversight of clinical projects. Activities include:Ensuring implementation of the scope of work, handover from Business Development to Clinical Project Manager, including Clinical Trial Management System (CTMS) set-up.Overseeing the implementation of CTMS in the Clinical Department including training requirements and project implementation,Ensuring development and implementation of project plans, communication plans, Training plans, TMF plans and other plans as required by the project.Reviewing of contracts for subcontracted services.Providing out of office /holiday cover for Clinical Project Manager(s).Performing interim Project Management of individual projects as required.Developing standard templates for project management tools. Overseeing the performance of projects against budget and milestones and report on performance to Director of Clinical Research and Managing Director.Day to day management of Clinical Project Managers and Clinical Team Leads to ensure that project milestones are met, including:Resource allocation with in the Clinical DepartmentReview of project status reports, attending project updates and reviewing minutes.First point of contact for escalation of issues by Clinical Project Managers and Clinical Team Leads.Mentoring and Staff Development within the Clinical Department.Identifying training needs and mentoring staff.Assist with forecasting of appropriate operational resource needs and budget for development of business.Additional company related duties as required. Show less

Project Manager• Plan and implement, to achieve, anticipated and unexpected project deliverables.• Analyse and oversee cost, personnel hours and project needs to determine the most cost effective and efficient means to run and complete projects successfully on time, to agreed quality standards and within budget while meeting the Customer’s needs and adhering to the contract.• Delegate assigned responsibilities to project team members.• Have regular and proactive liaisons with… Show more Project Manager• Plan and implement, to achieve, anticipated and unexpected project deliverables.• Analyse and oversee cost, personnel hours and project needs to determine the most cost effective and efficient means to run and complete projects successfully on time, to agreed quality standards and within budget while meeting the Customer’s needs and adhering to the contract.• Delegate assigned responsibilities to project team members.• Have regular and proactive liaisons with Department Heads to optimize performance and utilization of the project team members.• Anticipate potential issues and escalate appropriately/pro-actively to their Franchise Director/Associate Director.• Act as primary contact with Customer throughout study. Up to delivery of final project product(s). Show less

Having accepted an invitation to join the Board, as of 3rd November 2011 I am a Director of Revival Radio Limited the parent company of Revival FM. I continue to be a presenter on Scotland's only full-time Christian community radio station, 100.8 Revival Fm, broadcasting on 100.8 FM and on the web at www.revivalfm.orgMy programme, The Late Show, is braodcast each Wednesday evening between 21:30 and 23:30 UK time.I also present on selected other programmes including : Family… Show more Having accepted an invitation to join the Board, as of 3rd November 2011 I am a Director of Revival Radio Limited the parent company of Revival FM. I continue to be a presenter on Scotland's only full-time Christian community radio station, 100.8 Revival Fm, broadcasting on 100.8 FM and on the web at www.revivalfm.orgMy programme, The Late Show, is braodcast each Wednesday evening between 21:30 and 23:30 UK time.I also present on selected other programmes including : Family Favorites - Sundays between 14:00 and 16:00 UK time and The Saturday Breakfast Show, Saturdays between 07:00 and 10:00 UK time. Show less

Chair Steering Committee. Organize and contribute to agenda. Contact potential presenters and speakers. Chair Scottish Forum meetings. Lead discussion groups.

Global Process Advisor for “Study Site Management”. Global expertise in fielding questions relating to Study Site Management, reviewing and developing global procedures.Specific responsibility for Knowledge Management, liaison with the wider M&RA Directorate, AZ Global including representing the UK MC CRG on the Clinical Support Team (formerly the Clinical Process Management Advisory Group) and external organizations e.g. ICR/ICR Scotland forum. Global helpdesk, expert and co-ordination… Show more Global Process Advisor for “Study Site Management”. Global expertise in fielding questions relating to Study Site Management, reviewing and developing global procedures.Specific responsibility for Knowledge Management, liaison with the wider M&RA Directorate, AZ Global including representing the UK MC CRG on the Clinical Support Team (formerly the Clinical Process Management Advisory Group) and external organizations e.g. ICR/ICR Scotland forum. Global helpdesk, expert and co-ordination responsibility as part of global activity.Responsible for providing advice and training on AstraZeneca’s local and global clinical processes, SOPs, relevant IS/IT systems used for clinical trials and ICH-GCP. Contributing to the development, maintenance, improvement and implementation of local and global clinical processes and SOPs. Organising and conducting QC activities including accompanied field visits with CRS/CRA at study sites.Maintenance and development of relevant local information pages and database to ensure that staff have access to current information. Interfacing with Clinical Quality Assurance and Global functions (e.g. Global Learning Development, Global Skills Leaders, and Global Service Desks) as required.Providing leadership and support to the Clinical Process Management Team to deliver local implementation of global clinical processes, SOPs and systems and contribute to ongoing process development through the Clinical Process Management Advisory Group.Member of the Clinical Process Management Advisory Team. Responsible for providing advice and training on AstraZeneca’s local and global clinical processes, SOPs, relevant IS/IT systems used for clinical trials and ICH-GCP.Interfacing with Clinical Quality Assurance, Regional Training Advisor and Global functions (e.g. Global Training Network, Global Skills Leaders, and Global Service Desks) as required. Show less

Responsible for providing advice and training on AstraZeneca’s local and global clinical processes, SOPs, relevant IS/IT systems used for clinical trials and ICH-GCP.Contributing to the development, maintenance, improvement and implementation of local and global clinical processes and SOPs.Organising and conducting QC activities.Maintenance and development of relevant local information pages and databases to ensure that staff have access to current information.Interfacing with… Show more Responsible for providing advice and training on AstraZeneca’s local and global clinical processes, SOPs, relevant IS/IT systems used for clinical trials and ICH-GCP.Contributing to the development, maintenance, improvement and implementation of local and global clinical processes and SOPs.Organising and conducting QC activities.Maintenance and development of relevant local information pages and databases to ensure that staff have access to current information.Interfacing with Clinical Quality Assurance, Regional Training Advisor and Global functions (eg Global Training Network, Global Skills Leaders, and Global Service Desks) as required. Show less