Research Associate I

SAIC Frederick, Inc., the operations and technical support contractor for the NCI Frederick, has an excellent opportunity in our National Clinical Target Validation Lab.  You will be responsible for timely and accurate pick-up, labeling, transport, processing, storage and exact, detailed documentation of clinical research specimens. Requires clear verbal and written communication with clinical trial staff at the study sites and with laboratory staff who supervise the service. QC tasks will be assigned by the supervisor, which will involve routine checks of critical laboratory variables with documentation, data collection, and reports of findings to supervisors. Assignments are of a highly specialized nature and require attention to technical detail and accurate documentation in order to be carried out independently once trained by supervisor. Work involves potentially hazardous chemical and biological materials, and requires use of personal protective equipment and strict adherence to safety protocols. This position is primarily responsible for clinical specimens process and test and periodic flexibility in work hours is required.

Bachelor’s degree from an accredited college/university in a field related to biomedical research, clinical laboratory research, or laboratory medicine or four years experience in lieu of degree in the appropriate field required.  Foreign educated candidates who have completed part or all of their education outside of the United States must have their foreign education evaluated by an SAIC-approved accrediting organization to assure that it has met the equivalency of the qualifications of degree work in the United States. In addition to educational requirements, a minimum of two (2) years related biomedical experience in a clinical laboratory, lab medicine or hematology/pathology lab service, early clinical trial laboratory, or similar clinical lab environment. Must have demonstrated competence, knowledge, and experience in clinical specimen processing, accountability, documentation, reporting and confidentiality within a regulated/certified/accredited clinical laboratory environment such as CLIA, CAP, or cGCP.   Must be detail-oriented and conscientious with excellent organizational skills. Experience with clinical specimens that require specialized handling or processing as well as an ability to use PC based programs as part of daily routines required.  Must possess knowledge of basic subject matter, as well as experience and skill with basic laboratory techniques germane to processing and testing clinical specimens (i.e. pipetting, balance use, centrifuge use, safety procedures, etc.). This position is subject to obtaining a Public Trust Clearance.

For immediate consideration, please apply for position #141902 at our website http://saic-frederick.com

SAIC is an equal opportunity employer and values cultural diversity in the workplace.