Robert Rees

Robert Rees Email and Phone Number

Vice President, Clinical Science @ Nefro Avillion Clinical Development
Sunbury-on-Thames, GB
Robert Rees's Location
Sunbury-On-Thames, England, United Kingdom, United Kingdom
Robert Rees's Contact Details

Robert Rees work email

Robert Rees personal email

About Robert Rees

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.

Robert Rees's Current Company Details
Nefro Avillion Clinical Development

Nefro Avillion Clinical Development

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Vice President, Clinical Science
Sunbury-on-Thames, GB
Robert Rees Work Experience Details
  • Nefro Avillion Clinical Development
    Vice President, Clinical Science
    Nefro Avillion Clinical Development
    Sunbury-On-Thames, Gb
  • Avillion Llp
    Senior Director, Clinical Programs
    Avillion Llp Nov 2018 - Present
    London, England, Gb
  • Avillion Llp
    Program Director
    Avillion Llp Jan 2017 - Nov 2018
    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.
  • Avillion Llp
    Global Project Manager
    Avillion Llp Sep 2014 - Dec 2016
    London, England, Gb
    Global Project Manager working in Chronic Myeloid Leukaemia (Bosutinib, BFORE Trial)
  • Eli Lilly And Company
    Global Clinical Trials Manager (Fte)
    Eli Lilly And Company Sep 2012 - Sep 2014
    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.
  • Eli Lilly And Company
    Global Clinical Trials Manager (Contract)
    Eli Lilly And Company Oct 2010 - Sep 2012
    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.
  • Amgen
    Global Study Manager
    Amgen Jan 2009 - Oct 2010
    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.
  • Parexel
    Clinical Research Associate Ii (Cra Ii)
    Parexel Nov 2007 - Jan 2009
    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.
  • Prn, Basingstoke
    Clinical Research Associate
    Prn, Basingstoke Jun 2006 - Nov 2007
    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.

Robert Rees Skills

Clinical Trials Oncology Clinical Research Gcp Pharmaceutical Industry Diabetes Clinical Development Immunology Hematology Ctms Biotechnology Clinical Monitoring Ich Gcp Cardiology Pain Endocrinology

Robert Rees Education Details

  • University Of Bath
    University Of Bath
    Microbiology/Genetics
  • The University Of Edinburgh
    The University Of Edinburgh
    Microbiology
  • Madras College, St Andrews
    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.

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