Richard Seals
Study Director @Inotiv
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WORK HISTORY
Study Director @Inotiv
Mount Vernon, IN, US
Serve as Study Director as set forth in 21 Code of Federal Regulations Part 58. Conduct acute, chronic, and carcinogenicity studies for sponsors. Responsible for all phases of protocol development; communicating with: supervisory staff to establish a study schedule, the sponsor to finalize the protocol and the technical staff to coordinate study initiation. Direct and/or supervise the work of technical staff in accordance with the appropriate regulations and guidelines (including FDA, EPA, and OECD GLPs). Monitor the progress of studies and report the results to the sponsor. Carefully interprets study data to determine test article related effects, and assigns NOAEL and LOAEL values, when appropriate. Participate in in-house training programs for the technical staff. Conduct literature and/or Internet searches in support of protocol or report preparation. Prepare reports, papers and/or charts of study data for interim reports to the sponsor. Prepare posters and/or scientific papers.
EDUCATION
University of Tennessee, Knoxville
BS, Animal Science
Virginia Tech
PhD, Animal Science (Reproductive Physiology)
University of Tennessee, Knoxville
MS, Animal Science (Reproductive Physiology)
SKILLS
ABOUT RICHARD SEALS
A board certified toxicologist with over 18 years of experience conducting pharmaceutical research. Knowledge of appropriate guidelines and regulations. Project manager with the ability to work independently, learning new concepts to meet or exceed challenging deadlines, while working successfully in a high stress environment. A recognized leader working collaboratively within a team. Proven work history in delivering high quality results on time or in advance of projected deadlines and within budget. Skilled communicator and presenter both regionally and nationally. Successful author and editor of complex regulatory documents and scientific publications.
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