Location: Bethesda, MD
Founded in 1979, Technical Resources International, Inc. (TRI) provides a unique range of support services
in the areas of Communications, Health and Information Technology to both private industry and government agency clients. TRI is currently seeking a dedicated team player to join our Bethesda, MD team.
This position involves preparing scientific and regulatory documents on behalf of government and private sector clients for submission to the Food and Drug Administration (FDA) (Investigational New Drug applications, annual reports, preclinical and clinical study reports, safety reports, and Investigator’s Brochures); performing literature searches; preparing and editing manuscripts, meeting reports and proceedings, and safety documents; and data analysis.
Requirements include an M.S. degree or equivalent with 3 or more years of relevant work experience or a Ph.D. in pharmacology, biochemistry, molecular biology, immunology, or a related field; oncology and/or immunology background highly desirable. Requires excellent oral, written, data interpretation, and computer skills (experience with PC-based systems and MS Office required) and high attention to detail; familiarity with database design, FDA regulations, and/or clinical research highly desirable.
Submit resume and salary requirements to: Attn: TS, TRI, 6500 Rock Spring Dr., Suite 650, Bethesda, MD 20817, or fax to (301) 897-7401, or email to [Click Here to Email Your Resumé].
Technical Resources International is fully committed to Equal Employment Opportunity and to attracting, retaining, developing and promoting the most qualified employees without regard to their race, gender, color, religion, national origin, age, physical or mental disability, veteran status, or any other characteristic prohibited by state or local law.