Provide leadership to effectively coordinate the activities of a program of studies, project managers and sub-teams in a manner that ensures all time-frames and targets are met and costs are managed- Oversight of contracts, finances and vendors - Responsible for UK early phase oncology site network

Manage Study & Site Start up, Regulatory Affairs, Drug Supply, Pharmacovigilence, Clinical Monitoring, Data Management, Medical Consulting and third party vendors including Central Laboratories, Central Imaging Review, IxRS and electronic Patient Reported Outcomes* Focal point for client communication including proposal writing, agreeing, tracking and meeting timelines, contract negotiation, all aspects of project finances and quality control* Organise Investigator Meetings in different regions. Prepare and present at internal and external meetings* Ensure work is conducted in compliance with standard processes, policies and procedures and meets quality and timeline metrics

• Tumour genetics outsourcing management• Established collaborations with global laboratories in 5 different regions to provide biomarker data for Phase III oncology clinical trials.• Provided training and advice for the set up of biomarker laboratories in China and India• Managed QC of externally generated clinical trial data.• Prepared genetic analysis plans for oncology compounds• Worked with clinical QA to audit external vendors• Established an internal methylation analysis capability and managed a project to identify subgroups of breast and ovarian cancer patients, in order to enrich the patient population for clinical trials• Project managed delivery of internal oncology biomarker clinical trial data