Robert Rees Email & Phone Number

Sunbury-On-Thames, Gb

London, England, Gb

London, England, Gb

Lead implementation of clinical trials and programs. Interface with vendors, ensure data quality, manage clinical budgets and provide study operational expertise. Conduct due diligence for potential projects from a scientific and operational perspective.

London, England, Gb

Global Project Manager working in Chronic Myeloid Leukaemia (Bosutinib, BFORE Trial)

Indianapolis, Indiana, Us

Lead Global manager on high priority Phase III and safety trials within the Diabetes TA. Experience of development, maintenance and close-out with expertise in coordination of all activities, functions & partnerships required to successfully develop and implement complex Clinical Trials. Additional responsibilities include participation on vendor oversight committee to streamline operational integration with TPOs across all TAs in the EU.

Indianapolis, Indiana, Us

Lead Global manager on Phase II - III trials. Experience included data review, safety review, coordination of several successful database locks, CSR completion and publications reviews in study close-out. Study start-up experience included feasibility planning, milestone planning, protocol development and budget development and approval.

Thousand Oaks, Ca, Us

Manager in autoimmune condition Idiopathic Thrombocytopenic Purpura (ITP). Involved in all aspects of start-up, implementing and maintenace of a clinical trial at the global level. Experience included review and approval of vendor scope of work, milestone and budget planning. Planning and implementation of Investigator study training meetings and global study initiation.

Durham, North Carolina, Us

I exclusively worked on studies for one of the world's largest pharmaceutical companies. Therapeutic experience included; Colorectal cancer, Prostate cancer, Breast cancer, Ewings sarcoma, Diabetic Peripheral Neuropathy, and Fibromyalgia in Phase I - III. Lead CRA for a contraceptive Phase I medical device study and had the top two recruiting sites on a key registration study for Breast Cancer. Also assisted in the training of junior CRAs.

I have been involved in the monitoring of a number of studies, both in the UK and the EU. I have experience of studies using several online databases for electronic data capture, meeting recruitment targets, discrepancy resolution and dealing with SAEs. I have been involved in the set-up of several new studies and my responsibilities have included; completion and submission SSIs for ethics, PCT and R&D trust approvals, investigator identification and selection, obtaining confidentiality agreements, study feasibility and conducting site evaluation visits.

2006 Ph.D, Microbiology/Genetics

B.Sc. Hons (1St Class), Microbiology

Education record