B.S. or B.A. degree or equivalent related experience, 2-5 years regulatory or relevant work experience, Excellent oral, written, interpersonal and organizational skills, Solid computer skills; experience using Microsoft Office; Medical background preferred. Exposure to GCPs and clinical trials is a must.
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.
Founded in 1979, Technical Resources International, Inc. (TRI) is a full-service contract research organization plus (CRO+) providing product development support services to the global drug, biologic, and medical device community through the effective combination of scientific, clinical information technology, and communications services. TRI, Inc. is currently seeking a Task Area Manager/Clinical Information Specialist.
Primary responsibilities include the receipt and abstraction of protocol and/or contact information into the appropriate databases for use by the client and their collaborators in support of clinical trials; respond to phone or email queries regarding standard processes associated with the abstractions; assist in the preparation of contract required reports; participate in the revision of SOPs and work instructions as necessary and appropriate; Handle special client requests as assigned; Other duties as assigned.