Posted in Other about 11 hours ago.
Site: The Brigham and Women's Hospital, Inc.
At Mass General Brigham, we know it takes a surprising range of talented professionals to advance our mission-from doctors, nurses, business people and tech experts, to dedicated researchers and systems analysts. As a not-for-profit organization, Mass General Brigham is committed to supporting patient care, research, teaching, and service to the community. We place great value on being a diverse, equitable and inclusive organization as we aim to reflect the diversity of the patients we serve.
At Mass General Brigham, we believe a diverse set of backgrounds and lived experiences makes us stronger by challenging our assumptions with new perspectives that can drive revolutionary discoveries in medical innovations in research and patient care. Therefore, we invite and welcome applicants from traditionally underrepresented groups in healthcare - people of color, people with disabilities, LGBTQ community, and/or gender expansive, first and second-generation immigrants, veterans, and people from different socioeconomic backgrounds - to apply.
Job Summary
GENERAL SUMMARY/ OVERVIEW STATEMENT:
Serves as a member of a team dedicated to coordinating patient specimens for the Translational Biomarker Core (TBC), a research core within the Center for Advanced Molecular Diagnostics (CAMD) in the Department of Pathology.
Reporting to the CAMD Supervisor, this position is responsible for supporting the CAMD TBC. Responsibilities will include receiving, accessioning, coordinating and tracking orders and specimens through the Partners Core Management system and interacting with PIs throughout the institution to ensure successful completion of research projects. The position also includes laboratory duties including sample preparation and nucleic acid isolations.
Qualifications
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Responsibilities as Outlined by CLIA (as described in the Federal Register, 42 CFR, Subpart M 493.1403 - 1495.)
The testing personnel are responsible for specimen processing, test performance and for reporting test results.
(a) Each individual performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities.
(b) Each individual performing high complexity testing must-
(1) Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results;
(2) Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens;
(3) Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed;
(4) Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance;
(5) Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the general supervisor, technical supervisor, clinical consultant, or director;
(6) Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications; and
(7) Except as specified in paragraph (c) of this section, if qualified under § 493.1489(b)(5), perform high complexity testing only under the onsite, direct supervision of a general supervisor qualified under § 493.1461.
1. Under supervision from the CAMD Supervisor and Senior Research Scientist:
Receives service requests for CAMD TBC lab services through the Partners Core Management system.
Communicates with TBC users to coordinate sample submission.
Evaluates sample submissions and requisition information and accessions cases into the Anatomic Pathology laboratory information system (LIS), PowerPath
Receives samples, verifies, and gathers patient and test information as needed
Documents information associated with patient specimens, testing, and inquiries
Troubleshoots basic problems related to specimen and patient information
Works with laboratory technologists to facilitate research sample testing
Maintains research project tracking spreadsheets
Assigns research OncoPanel cases to pathologists for sign out
Uploads signed out research OncoPanel reports to OneDrive and notifies PI that results are available
Tracks project progress and completes service requests upon study completion
Some sample preparation lab work may be required
Maintains Core reagent inventory
Under supervision from the CAMD Supervisor and Technical staff:
Performs laboratory duties that include tissue processing, nucleic acid extraction, and quantification according to laboratory policies and procedures
Records sample data and progression through the laboratory in laboratory information management system (LIMS) and/or sample tracking spreadsheets
Performs other laboratory work that may include instrument quality control, preparation and processing of samples, preparation of laboratory reagents, maintenance of reagent and supply inventory, and other tasks.
May perform relevant literature searches for the CAMD Research core
Maintains established department policies, procedures and objectives, including the areas of quality assurance, safety, environmental and infection control.
Performs all other duties and responsibilities as directed.
Qualifications - External
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