Clinical Lab Technologist I, Pathology

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.

• Bachelor's Degree and an interest in clinical research.
• 0- 1 year prior experience in a healthcare setting.
• Experience with MS Office 365 applications, including Word, Excel, and PowerPoint.
• Familiarity of medical terminology preferred.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

• Must possess excellent organizational skills and ability to prioritize work appropriately.
• Ability to methodically record data with a very high level of accuracy.
• Good interpersonal skills to interact effectively with co-workers, department staff, and principle investigators
• Strong computer skills with specific knowledge of Microsoft Office 365: Word , Excel and PowerPoint
• Ability to work in a fast-paced dynamic work environment
• Ability to work collaboratively with a team
• Must be able to handle confidential patient information with absolute discretion and sound judgment

WORKING CONDITIONS:

• Busy clinical laboratory environment.
• Exposure to blood and other body fluids.
• Work requires frequent standing, walking and/or occasional lifting or carrying of supplies.
• Noise level is high due to continuous operation of lab equipment.

HOSPITAL WIDE RESPONSIBILITIES:

Works within legal, regulatory, accreditation and ethical practice standards relevant to the position and as established by BWH/Partners; follows safe practices required for the position; complies with appropriate BWH and Partners policies and procedures; fulfills any training required by BWH and/or Partners, as appropriate; brings potential matters of non-compliance to the attention of the supervisor or other appropriate hospital staff.