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Clinical trialist physician and clinical pharmacologist with 15+ years of drug-development experience in phases I, II and III. Initially, conducted significant portions of the full development program and authored several of the regulatory documents that led to the world-wide approval of an ARB for hypertension. Later, responsible for the successful introduction into man of approximately 5 metabolic, neuroscience and CV NCEs per year. Led multiple cross-functional Early Development Teams for CV and Metabolics compounds. Managed departmental grant budgets up to $10 million and a staff of up to 50 health care professionals. 40 peer-reviewed publications. Board-certified physician.Specialties: Clinical trial design and conduct, including TQT studies. Authoring and critiquing clinical summaries for regulatory submission and AdCom presentations.
Rar Consulting, Llc
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PresidentRar Consulting, Llc Jan 2008 - PresentPennington, NjOffering expertise in Phase I and Phase II/III clinical drug development and related regulatory document writing and representation at FDA meetings.Projects in the last year have included design of a phase IIa study for a cholesterol-lowering drug, PK/PD analysis to support FIH dose selection and rationales for FIH sections of protocols, advice on pursuing two generic drug registration programs for FDA, consultant mentoring of PhD's in the clinical aspects of early drug development, particularly clinical pharmacology, safety monitoring and regulatory challenges; and publications of recent results and peer review for clin pharm journals.
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MemberAmerican Society Of Clinical Pharmacology 1981 - Present
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Executive DirectorBristol-Myers Squibb Nov 1992 - Dec 2007Led the CV/Metabolics/Neuroscience division of BMS' clinical pharmacology/experimental medicine department, with approximately five First-in-human starts and 25-40 clinical pharmacology studies/year (including proof-of-concept, drug metabolism/PK, QT/QTc studies and special populations). Managed departmental grant budgets up to $10 million and a staff of up to 50 health care professionals. Led 5 Early Development Cross-functional teams (membership drawn from 9 departments); responsible for the Early Clinical Development Plan and execution of all required components to successfully move through IND and First-in human to proof of concept. Member of the First-in-human Committee. -
Assistant ProfessorUniversity Of Toronto 1983 - 1992Research in clinical hypertension focusing on potential utility of ABPM and echocardiography for better diagnosis; funded by the Ontario Ministry of Health and the Ontario Heart Foundation, and career support from the Medical Research Council-Pharmaceutical Manufacturers’ Association of Canada. -
Staff PhysicianSunnybrook Medical Centre 1983 - 1992Responsible for medical care and teaching on a general medicine ward, including the initial cases of AIDS. Rana tertiary referral Hypertension Clinic and research program.
Richard Reeves Skills
Richard Reeves Education Details
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Md, Cm -
Pre-Med -
Physics -
Medicine
Frequently Asked Questions about Richard Reeves
What company does Richard Reeves work for?
Richard Reeves works for Rar Consulting, Llc
What is Richard Reeves's role at the current company?
Richard Reeves's current role is President at RAR Consulting, LLC - now retired..
What is Richard Reeves's email address?
Richard Reeves's email address is ra****@****ast.net
What is Richard Reeves's direct phone number?
Richard Reeves's direct phone number is (203)-677*****
What schools did Richard Reeves attend?
Richard Reeves attended University Of Pittsburgh School Of Medicine, Mcgill University, The George Washington University, Pennsylvania State University, Mcgill University.
What are some of Richard Reeves's interests?
Richard Reeves has interest in Education.
What skills is Richard Reeves known for?
Richard Reeves has skills like Clinical Trials, Clinical Development, Pharmaceutical Industry, Clinical Research, Medical Writing, Drug Development, Regulatory Submissions, Clinical Pharmacology, Health Economics, Neurology, Pharmacology, Regulatory Affairs.
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Richard Reeves
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