Robert Rees Email and Phone Number
Robert Rees work email
- Valid
Robert Rees personal email
- Valid
A highly qualified scientist and skilled clinical development professional. Extensive experience of implementing successful late phase clinical development programmes and supporting marketing applications. Expertise in assessment of clinical phase drug development pipeline candidates from a due diligence and investment perspective. Specialties include: strategic alliance management, clinical pipeline review and due diligence, budget and contract negotiation, vendor relations, design and implementation of clinical development plans, regulatory strategy, management of large cross functional and cross organisational teams, risk assessment, feasibility planning, protocol development, review and analysis of big data, safety review and clinical study reporting.
-
Vice President, Clinical ScienceNefro Avillion Clinical DevelopmentSunbury-On-Thames, Gb
-
Senior Director, Clinical ProgramsAvillion Llp Nov 2018 - PresentLondon, England, Gb -
Program DirectorAvillion Llp Jan 2017 - Nov 2018London, England, GbLead 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. -
Global Project ManagerAvillion Llp Sep 2014 - Dec 2016London, England, GbGlobal Project Manager working in Chronic Myeloid Leukaemia (Bosutinib, BFORE Trial) -
Global Clinical Trials Manager (Fte)Eli Lilly And Company Sep 2012 - Sep 2014Indianapolis, Indiana, UsLead 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. -
Global Clinical Trials Manager (Contract)Eli Lilly And Company Oct 2010 - Sep 2012Indianapolis, Indiana, UsLead 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. -
Global Study ManagerAmgen Jan 2009 - Oct 2010Thousand Oaks, Ca, UsManager 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. -
Clinical Research Associate Ii (Cra Ii)Parexel Nov 2007 - Jan 2009Durham, North Carolina, UsI 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. -
Clinical Research AssociatePrn, Basingstoke Jun 2006 - Nov 2007I 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.
Robert Rees Skills
Robert Rees Education Details
-
University Of BathMicrobiology/Genetics -
The University Of EdinburghMicrobiology -
Madras College, St Andrews
Frequently Asked Questions about Robert Rees
What company does Robert Rees work for?
Robert Rees works for Nefro Avillion Clinical Development
What is Robert Rees's role at the current company?
Robert Rees's current role is Vice President, Clinical Science.
What is Robert Rees's email address?
Robert Rees's email address is bo****@****ail.com
What schools did Robert Rees attend?
Robert Rees attended University Of Bath, The University Of Edinburgh, Madras College, St Andrews.
What are some of Robert Rees's interests?
Robert Rees has interest in Education.
What skills is Robert Rees known for?
Robert Rees has skills like Clinical Trials, Oncology, Clinical Research, Gcp, Pharmaceutical Industry, Diabetes, Clinical Development, Immunology, Hematology, Ctms, Biotechnology, Clinical Monitoring.
Free Chrome Extension
Find emails, phones & company data instantly
Aero Online
Your AI prospecting assistant
Select data to include:
0 records × $0.02 per record
Download 750 million emails and 100 million phone numbers
Access emails and phone numbers of over 750 million business users. Instantly download verified profiles using 20+ filters, including location, job title, company, function, and industry.
Start your free trial