Research Technician, CGR, NCI Connect Study (Tues-Sat)

Job ID: req4649 Employee Type: nonexempt full-time Division: Clinical Research Directorate Facility: Rockville: 9615 MedCtrDr Location: 9615 Medical Center Drive, Rockville, MD 20850 USA The Frederick National Laboratory is operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases. Accountability, Compassion, Collaboration, Dedication, Integrity and Versatility; it's the FNL way. Program Description The BioProcessing and Trial Logistics (BPTL) functional team within the Cancer Genomics Research Laboratory (CGR) plays a critical role in supporting the National Cancer Institute (NCI) Division of Cancer Epidemiology and Genetics (DCEG) through expert oversight of biospecimen operations for a variety of research aims. By integrating laboratory operations, biospecimen processing, inventory management, and site coordination, BPTL helps ensure that specimens are collected, processed, stored, tracked, and documented with the highest standards of quality and integrity. We are seeking a Research Technician (Tuesday – Saturday) to provide biospecimen processing support for the DCEG Connect for Cancer Prevention study. Key Roles/Responsibilities Execute biospecimen processing workflows under established SOPs, including receipt, processing, aliquoting, and appropriate storage of created aliquots. Work effectively in a BSL-2 environment to process and create biospecimen resources for current and future research aims, including blood fractionation, isolation of buccal cells from mouthwash and urine processing. Process additional specimen types as CONNECT study aims and workflows evolve in accordance with established SOPs (e.g. home fecal collections for microbiome research). Record accurate and timely biospecimen details within laboratory databases or other documentation systems, including specimen receipt information and processing documentation Purposeful and consistent adherence to existing SOPs to ensure that time-sensitive specimens are handled according to established protocols Support continuous improvement of laboratory workflows using CGR’s established quality management systems and operational infrastructure including documentation of deviations Adhere to existing laboratory quality assurance guidelines, equipment and supply management protocols, and general laboratory organization activities Use of Excel, Word, Outlook and other laboratory information systems daily for tracking, reporting and communication Basic Qualifications Bachelor’s degree from an accredited college/university recognized by the Council for Higher Education Accreditation (CHEA) in a field related to biomedical research, or four (4) years of relevant experience in lieu of degree. Foreign degrees must be evaluated for U.S. equivalency No work experience required with a Bachelors degree Understanding of biospecimen handling and documentation requirements Strong interpersonal and cross-cultural communication skills, with the ability to work effectively with internal leadership Experience with Microsoft Office Suite, including Excel, Word, Teams, and Outlook Ability to maintain focus for extended periods of time and manage detailed data entry accurately Ability to work temporarily in Frederick, MD during the office transition to Rockville, MD Ability to obtain and maintain a security clearance Preferred Qualifications Experience in biospecimen processing and specimen inventory Experience working with human biological specimens in research, clinical, or biorepository setting including blood fractionation Knowledge of aseptic techniques in human biospecimen processing Experience with biospecimen inventory management databases, laboratory information management systems (LIMS), or electronic laboratory notebooks (ELNs) Familiarity with quality management systems in a regulated or high-throughput laboratory environment JOB HAZARDS This position is subject to working with or has the potential for exposure to infectious material, requiring medical clearance and immunizations Commitment to Non-Discrimination All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, color, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws. Pay And Benefits Pay and benefits are fundamental to any career decision. That's why we craft compensation packages that reflect the importance of the work we do for our customers. Employment benefits include competitive compensation, Health and Wellness programs, Income Protection, Paid Leave and Retirement. More details are available here

43,800.00 - 62,702.00 USD

The posted pay range for this job is a general guideline and not a guarantee of compensation or salary. Additional factors considered in extending an offer include, but are not limited to, responsibilities of the job, education, experience, knowledge, skills, and abilities as well as internal equity, and alignment with market data. The salary range posted is a full-time equivalent salary and will vary depending on scheduled hours for part time positions #J-18808-Ljbffr BioSpace