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Clinical Lab Scientist

Iazuqy Fa Ocs Oraclecloud Com CX 1 · San Francisco, CA, United States; Moffitt Hospital - FL 05 - RM M547, San Francisco, CA, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
TitleClinical Lab Scientist
Normalized title-
Department / teamClinical Laboratory Services
LocationSan Francisco, CA, United States
Work model-
Employment type-
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-06-03 / 2026-06-04
Changed / last seen2026-06-06 / 2026-06-06

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Linked records

CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
Source1ec01ec1-9ec0-4ca7-9242-3de42049e519
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description Job Function Summary: Serve the needs of adult patients cared for by the UCSF Hematology, Blood and Marrow Transplant, and Cellular Therapy Program. Perform procedures related to the processing, storage and distribution of cellular therapy products, to include Bone Marrow, Stem Cell, and Immune Effector Cell products. Performs test procedures in the Adult Cell Therapy Lab to include flow cytometry. Transcribes and reports test results. Operates laboratory instrumentation & equipment to accurately generate test results. Initiates troubleshooting of errant laboratory instrumentation & equipment as needed. Follows established quality control procedures and participate in all associated tasks in the section. Responsibilities Key Responsibilities % of time Essential Function (Yes/No) Key Responsibilities 50 Yes To perform procedures related to cellular therapy processing Performs all procedures assigned to the shift in an accurate and efficient manner. Learns and performs any new procedure within a reasonable time frame. Performs procedures in a manner, which does not deviate from the step-by-step procedure write-up. Any deviation from the procedure must be reviewed with a supervisor prior to sending any results. Be responsible for procedural updates by reviewing procedures on an annual basis, checking posted and emailed updates, and by reading and initialing all meeting notes. Completes test procedures and transmits results in the laboratory computer system within established turn-around times (TATs). Reviews results and validates on computer screen before releasing the results to the LIS (Laboratory Information System). Never alters patient test results in any way after they have been released to the LIS except through accepted procedure with documentation. Labels specimens, reagents and worksheets with required information in a legible and neat manner with ink pen. Completes required training and competency assessments within the assigned time frames. Maintains a clean and neat work area. Replenish supplies and prepare reagents as needed. Wears buttoned lab coat, gloves and uses face protection when handling patient samples. Exercises proper care and precautions to protect oneself from health hazards. Refrains from smoking, drinking, or eating in and around work areas. Take full responsibility for errors when committed, notifies required personnel and completes appropriate documentation. Integrates assigned tasks in order to complete the assignments by the end of the work shift. Works well without close or continual supervision. Accepts a reasonable increase in the workload when necessary or assigned by a supervisor. Adheres to all policies and procedures established in the Clinical Laboratory Personnel Policies. Performs special studies or projects when added to routine procedure run or when assigned separately. Process, cryopreserve and distribute all types of cellular therapy products Perform sterility cultures and dispense specimens to appropriate locations. Follow-up results of sterility and document in the appropriate worksheet. Verify the physician’s order for transplant and coordinate thaw time with the physician or nurse practitioner. Review donor eligibility determination before the collection day. Follow-up with the nurse coordinator any missing information and report to the supervisor or designee any problem with donor eligibility. Recognize and solve problems, exercising sound judgment to ensure optimal recovery of the cellular therapy products. Thaw the cellular therapy products following the thawing procedure. Receive and transport cellular therapy products accurately by following the existing procedure for shipping and receiving including following the National Marrow Donor Program. Perform nucleated cell count using automated cell counter. Perform CD34, CD3 and 7AAD analysis for cellular therapy products (as applicable). Gate and Analyze the CD34/CD3 population using the Flow analyzer. 35 Yes To assist in and ensure smooth operation of the BMT Lab operation Keep all equipment and other supplies clean, organized, and in proper order in the BMT laboratory. Maintain adequate inventory levels of supplies. Notify the supervisor of any short supply, short dated, or outdated supplies. Maintain equipment in good working order, including adequate liquid nitrogen levels in storage tanks. Perform alarm quality control on all the storage tanks according to schedule. Monitor and maintain records for quality control of techniques, reagents, tests and equipment. Maintain computer data entry and retrieval system, including engraftment data, bone marrow and aliquot sample inventory, and patient inventory. Accurately discard or issue for research cellular therapy products that have been signed off to be discarded by the attending physician. Ensure that patients are appropriately flagged in the Clinical Lab computer with regards to need for irradiated blood products, and products having specific blood types. Teach residents, fellows and CLS students about ACTL procedures To act as lab liaison with Bone Marrow Transplant team and with the nursing units. Attend the Adult Bone Marrow Conference Meeting as scheduled by the supervisor. Appropriately and accurately write the patients transplant and collections schedule date on the calendar. Follows cGMP (current Good Manufacturing Practices) in all procedures and in record keeping. 10 Yes Analyze designated quality control material with all procedures Analyzes required quality control material for all procedures. Records QC results on worksheet and/or in the LIS. Repeats test run if controls are outside the posted control range. Initiate troubleshooting of out-of-control situations. Notifies a supervisor whenever results of assays on QC materials are out-of-range. Completes analysis of proficiency testing material within stated turn-around-time. 5 Yes Perform additional duties, projects, and/or special assignments when requested. Initiates Laboratory Problem Reports or Incident Reports to document complaints, errors, injuries and/or variances from standard procedure. Perform special projects such as validation, Audits, Quality Indicators and other data as instructed by the supervisor within the agreed upon time period. Provide and maintain statistics, as instructed by the supervisor 100% Qualifications REQUIRED QUALIFICATIONS: This position requires flexibility to orient and work in all UCSF Medical Center locations as needed. College graduate with a BA/BS in a related science. Good Technical Skills. Ability to make sound decisions and good judgment. Must have high level of awareness for unusual or abnormal results and good problem solving skills. Must have strong interpersonal skills and relate to supervisors and co-workers. Must have excellent communication skills. Must produce accurate, complete, legible records of work performed. PREFERRED QUALIFICATION: Prefer 2 years’ experience in Cellular Therapy, Blood and Marrow Processing Laboratory. Prefer 2 years’ experience in Blood Banking, Component Processing or Transfusion service within the past 5 years. Prefer thorough knowledge in the fields of Cellular Therapy Processing and Storage. Prefer recent experience in a clinical laboratory setting that handle blood products using aseptic technique, knowledge of cGMP and blood product component processing and isolation. REQUIRED LICENSES/CERTIFICATIONS: Current California Clinical Laboratory Scientist License (Medical Technology) - Generalist Company About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells. Pride Values UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as our PRIDE values . In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here . Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Salary Information The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement. To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

Full job record

Job ID6335edd3d8f18b0fe2ce7784ff3e0929b767f115
Org IDb73f2bf1-b0ab-47ed-8db1-1f14a038aa7c
Source ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Board ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Provideroracle_hcm
Provider Job Key3927
TitleClinical Lab Scientist
Normalized Title
Statusactive
Activeyes
Location TextSan Francisco, CA, United States; Moffitt Hospital - FL 05 - RM M547, San Francisco, CA, US
DepartmentClinical Laboratory Services
Team
Employment Type
Workplace Type
Remote Policy
CountryUnited States
RegionCA
CitySan Francisco
Salary RawDescription Job Function Summary: Serve the needs of adult patients cared for by the UCSF Hematology, Blood and Marrow Transplant, and Cellular Therapy Program. Perform procedures related to the processing, storage and distribution of cellular therapy products, to include Bone Marrow, Stem Cell, and Immune Effector Cell products. Performs test procedures in the Adult Cell Therapy Lab to include flow cytometry. Transcribes and reports test results. Operates laboratory instrumentation & equipment to accurately generate test results. Initiates troubleshooting of errant laboratory instrumentation & equipment as needed. Follows established quality control procedures and participate in all associated tasks in the section. Responsibilities Key Responsibilities % of time Essential Function (Yes/No) Key Responsibilities 50 Yes To perform procedures related to cellular therapy processing Performs all procedures assigned to the shift in an accurate and efficient manner. Learns and performs any new procedure within a reasonable time frame. Performs procedures in a manner, which does not deviate from the step-by-step procedure write-up. Any deviation from the procedure must be reviewed with a supervisor prior to sending any results. Be responsible for procedural updates by reviewing procedures on an annual basis, checking posted and emailed updates, and by reading and initialing all meeting notes. Completes test procedures and transmits results in the laboratory computer system within established turn-around times (TATs). Reviews results and validates on computer screen before releasing the results to the LIS (Laboratory Information System). Never alters patient test results in any way after they have been released to the LIS except through accepted procedure with documentation. Labels specimens, reagents and worksheets with required information in a legible and neat manner with ink pen. Completes required training and competency assessments within the assigned time frames. Maintains a clean and neat work area. Replenish supplies and prepare reagents as needed. Wears buttoned lab coat, gloves and uses face protection when handling patient samples. Exercises proper care and precautions to protect oneself from health hazards. Refrains from smoking, drinking, or eating in and around work areas. Take full responsibility for errors when committed, notifies required personnel and completes appropriate documentation. Integrates assigned tasks in order to complete the assignments by the end of the work shift. Works well without close or continual supervision. Accepts a reasonable increase in the workload when necessary or assigned by a supervisor. Adheres to all policies and procedures established in the Clinical Laboratory Personnel Policies. Performs special studies or projects when added to routine procedure run or when assigned separately. Process, cryopreserve and distribute all types of cellular therapy products Perform sterility cultures and dispense specimens to appropriate locations. Follow-up results of sterility and document in the appropriate worksheet. Verify the physician’s order for transplant and coordinate thaw time with the physician or nurse practitioner. Review donor eligibility determination before the collection day. Follow-up with the nurse coordinator any missing information and report to the supervisor or designee any problem with donor eligibility. Recognize and solve problems, exercising sound judgment to ensure optimal recovery of the cellular therapy products. Thaw the cellular therapy products following the thawing procedure. Receive and transport cellular therapy products accurately by following the existing procedure for shipping and receiving including following the National Marrow Donor Program. Perform nucleated cell count using automated cell counter. Perform CD34, CD3 and 7AAD analysis for cellular therapy products (as applicable). Gate and Analyze the CD34/CD3 population using the Flow analyzer. 35 Yes To assist in and ensure smooth operation of the BMT Lab operation Keep all equipment and other supplies clean, organized, and in proper order in the BMT laboratory. Maintain adequate inventory levels of supplies. Notify the supervisor of any short supply, short dated, or outdated supplies. Maintain equipment in good working order, including adequate liquid nitrogen levels in storage tanks. Perform alarm quality control on all the storage tanks according to schedule. Monitor and maintain records for quality control of techniques, reagents, tests and equipment. Maintain computer data entry and retrieval system, including engraftment data, bone marrow and aliquot sample inventory, and patient inventory. Accurately discard or issue for research cellular therapy products that have been signed off to be discarded by the attending physician. Ensure that patients are appropriately flagged in the Clinical Lab computer with regards to need for irradiated blood products, and products having specific blood types. Teach residents, fellows and CLS students about ACTL procedures To act as lab liaison with Bone Marrow Transplant team and with the nursing units. Attend the Adult Bone Marrow Conference Meeting as scheduled by the supervisor. Appropriately and accurately write the patients transplant and collections schedule date on the calendar. Follows cGMP (current Good Manufacturing Practices) in all procedures and in record keeping. 10 Yes Analyze designated quality control material with all procedures Analyzes required quality control material for all procedures. Records QC results on worksheet and/or in the LIS. Repeats test run if controls are outside the posted control range. Initiate troubleshooting of out-of-control situations. Notifies a supervisor whenever results of assays on QC materials are out-of-range. Completes analysis of proficiency testing material within stated turn-around-time. 5 Yes Perform additional duties, projects, and/or special assignments when requested. Initiates Laboratory Problem Reports or Incident Reports to document complaints, errors, injuries and/or variances from standard procedure. Perform special projects such as validation, Audits, Quality Indicators and other data as instructed by the supervisor within the agreed upon time period. Provide and maintain statistics, as instructed by the supervisor 100% Qualifications REQUIRED QUALIFICATIONS: This position requires flexibility to orient and work in all UCSF Medical Center locations as needed. College graduate with a BA/BS in a related science. Good Technical Skills. Ability to make sound decisions and good judgment. Must have high level of awareness for unusual or abnormal results and good problem solving skills. Must have strong interpersonal skills and relate to supervisors and co-workers. Must have excellent communication skills. Must produce accurate, complete, legible records of work performed. PREFERRED QUALIFICATION: Prefer 2 years’ experience in Cellular Therapy, Blood and Marrow Processing Laboratory. Prefer 2 years’ experience in Blood Banking, Component Processing or Transfusion service within the past 5 years. Prefer thorough knowledge in the fields of Cellular Therapy Processing and Storage. Prefer recent experience in a clinical laboratory setting that handle blood products using aseptic technique, knowledge of cGMP and blood product component processing and isolation. REQUIRED LICENSES/CERTIFICATIONS: Current California Clinical Laboratory Scientist License (Medical Technology) - Generalist Company About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells. Pride Values UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as our PRIDE values . In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here . Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity The University of California is an Equal Opportunity Employer. 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First Seen At2026-06-04 10:20:52Z
Last Seen At2026-06-06 19:36:14Z
Last Checked At2026-06-06 19:36:14Z
Last Changed At2026-06-06 11:18:11Z
Inactive At
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    "ExternalQualificationsStr": "<div class=\"WordSection1\"><p>REQUIRED QUALIFICATIONS:</p><ul><li>This position requires flexibility to orient and work in all UCSF Medical Center locations as needed.</li><li>College graduate with a BA/BS in a related science.</li><li>Good Technical Skills.</li><li>Ability to make sound decisions and good judgment.</li><li>Must have high level of awareness for unusual or abnormal results and good problem solving skills.</li><li>Must have strong interpersonal skills and relate to supervisors and co-workers.</li><li>Must have excellent communication skills.</li><li><p>Must produce accurate, complete, legible records of work performed.</p><p>&nbsp;</p></li></ul><p>&nbsp;</p><p>PREFERRED QUALIFICATION:</p><ul style=\"list-style-type: disc;\"><li>Prefer 2 years’ experience in Cellular Therapy, Blood and Marrow Processing Laboratory.</li><li>Prefer 2 years’ experience in Blood Banking, Component Processing or Transfusion service within the past 5 years.&nbsp;</li><li>Prefer thorough knowledge in the fields of Cellular Therapy Processing and Storage.</li><li>Prefer recent experience in a clinical laboratory setting that handle blood products using aseptic technique, knowledge of cGMP and blood product component processing and isolation.</li></ul><p>&nbsp;</p><p>REQUIRED LICENSES/CERTIFICATIONS:</p><p>Current California Clinical Laboratory Scientist License (Medical Technology) - Generalist</p><p>&nbsp;</p></div>",
    "InternalQualificationsStr": "<div class=\"WordSection1\"><p>REQUIRED QUALIFICATIONS:</p><ul><li>This position requires flexibility to orient and work in all UCSF Medical Center locations as needed.</li><li>College graduate with a BA/BS in a related science.</li><li>Good Technical Skills.</li><li>Ability to make sound decisions and good judgment.</li><li>Must have high level of awareness for unusual or abnormal results and good problem solving skills.</li><li>Must have strong interpersonal skills and relate to supervisors and co-workers.</li><li>Must have excellent communication skills.</li><li><p>Must produce accurate, complete, legible records of work performed.</p><p>&nbsp;</p></li></ul><p>&nbsp;</p><p>PREFERRED QUALIFICATION:</p><ul style=\"list-style-type: disc;\"><li>Prefer 2 years’ experience in Cellular Therapy, Blood and Marrow Processing Laboratory.</li><li>Prefer 2 years’ experience in Blood Banking, Component Processing or Transfusion service within the past 5 years.&nbsp;</li><li>Prefer thorough knowledge in the fields of Cellular Therapy Processing and Storage.</li><li>Prefer recent experience in a clinical laboratory setting that handle blood products using aseptic technique, knowledge of cGMP and blood product component processing and isolation.</li></ul><p>&nbsp;</p><p>REQUIRED LICENSES/CERTIFICATIONS:</p><p>Current California Clinical Laboratory Scientist License (Medical Technology) - Generalist</p><p>&nbsp;</p></div>",
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    "ExternalResponsibilitiesStr": "<p style=\"break-after: avoid;\"><span style=\"font-size: 12pt;\"><strong>Key Responsibilities</strong></span><strong>&nbsp;</strong></p><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" width=\"655\" style=\"border-collapse: collapse; width: 491.4pt;\"><tbody><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">%&nbsp;</p><p style=\"text-align: center;\">of time</p></td><td width=\"71\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Essential Function (Yes/No)</p></td><td width=\"501\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 376.05pt;\"><p style=\"text-align: center;\">&nbsp;&nbsp;</p><p style=\"text-align: center;\">Key Responsibilities</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">50</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>To perform procedures related to cellular therapy processing</p><ol style=\"padding-left: 48px;\"><li>Performs all procedures assigned to the shift in an accurate and efficient manner.</li><li>Learns and performs any new procedure within a reasonable time frame.</li><li><p>Performs procedures in a manner, which does not deviate from the step-by-step procedure write-up. Any deviation from the procedure must be reviewed with a supervisor prior to sending any results.</p><p>&nbsp;</p></li><li>Be responsible for procedural updates by reviewing procedures on an annual basis, checking posted and emailed updates, and by reading and initialing all meeting notes.&nbsp;</li><li><p>Completes test procedures and transmits results in the laboratory computer system within established turn-around times (TATs).</p><p>&nbsp;</p></li><li>Reviews results and validates on computer screen before releasing the results to the LIS (Laboratory Information System).</li><li>Never alters patient test results in any way after they have been released to the LIS except through accepted procedure with documentation.&nbsp;</li><li>Labels specimens, reagents and worksheets with required information in a legible and neat manner with ink pen.</li><li>Completes required training and competency assessments within the assigned time frames.&nbsp;</li><li>Maintains a clean and neat work area. Replenish supplies and prepare reagents as needed.</li><li>Wears buttoned lab coat, gloves and uses face protection when handling patient samples. Exercises proper care and precautions to protect oneself from health hazards. Refrains from smoking, drinking, or eating in and around work areas.</li><li>Take full responsibility for errors when committed, notifies required personnel and completes appropriate documentation.&nbsp;</li><li>Integrates assigned tasks in order to complete the assignments by the end of the work shift.</li><li>Works well without close or continual supervision.</li><li><p>Accepts a reasonable increase in the workload when necessary or assigned by a supervisor.</p><p>&nbsp;</p></li><li>Adheres to all policies and procedures established in the Clinical Laboratory Personnel Policies.</li></ol><p>&nbsp;</p><ol start=\"17\" style=\"padding-left: 48px;\"><li><p>Performs special studies or projects when added to routine procedure run or when assigned separately.</p><p>&nbsp;</p></li><li><p>Process, cryopreserve and distribute all types of cellular therapy products</p><p>&nbsp;</p></li><li><p>Perform sterility cultures and dispense specimens to appropriate locations. Follow-up results of sterility and document in the appropriate worksheet.</p><p>&nbsp;</p></li><li><p>Verify the physician’s order for transplant and coordinate thaw time with the physician or nurse practitioner.&nbsp;</p><p>&nbsp;</p></li><li><p>Review donor eligibility determination before the collection day. Follow-up with the nurse coordinator any missing information and report to the supervisor or designee any problem with donor eligibility.</p><p>&nbsp;</p></li><li><p>Recognize and solve problems, exercising sound judgment to ensure optimal recovery of the cellular therapy products.</p><p>&nbsp;</p></li><li><p>Thaw the cellular therapy products following the thawing procedure.&nbsp;</p><p>&nbsp;</p></li><li>Receive and transport cellular therapy products accurately by following the existing procedure for shipping and receiving including following the National Marrow Donor Program.</li><li>Perform nucleated cell count using automated cell counter.</li><li>Perform CD34, CD3 and 7AAD analysis for cellular therapy products (as applicable). Gate and Analyze the CD34/CD3 population using the Flow analyzer.&nbsp;</li></ol><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">35</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>To assist in and ensure smooth operation of the&nbsp;BMT Lab operation</p><ol style=\"padding-left: 96px;\"><li><p>Keep all equipment and other supplies clean, organized, and in proper order in the BMT laboratory. Maintain adequate inventory levels of supplies. Notify the supervisor of any short supply, short dated, or outdated supplies.</p><p>&nbsp;</p></li><li>Maintain equipment in good working order, including adequate liquid nitrogen levels in storage tanks. Perform alarm quality control on all the storage tanks according to schedule.</li><li>Monitor and maintain records for quality control of techniques, reagents, tests and equipment.</li><li>Maintain computer data entry and retrieval system, including engraftment data, bone marrow and aliquot sample inventory, and patient inventory.</li><li>Accurately discard or issue for research cellular therapy products that have been signed off to be discarded by the attending physician.</li><li>Ensure that patients are appropriately flagged in the Clinical Lab computer with regards to need for irradiated blood products, and products having specific blood types.</li><li>Teach residents, fellows and CLS students about ACTL procedures</li><li>To act as lab liaison with Bone Marrow Transplant team and with the nursing units.</li><li>Attend the Adult Bone Marrow Conference Meeting as scheduled by the supervisor.&nbsp;</li><li>Appropriately and accurately write the patients transplant and&nbsp; &nbsp;collections schedule date on the calendar.</li><li><p>Follows cGMP (current Good Manufacturing Practices) in all procedures and in record keeping.</p><p>&nbsp;</p></li></ol></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">10</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>Analyze designated quality control material with all procedures</p><ol><li>Analyzes required quality control material for all procedures.&nbsp;</li><li>Records QC results on worksheet and/or in the LIS.</li><li>Repeats test run if controls are outside the posted control range. Initiate troubleshooting of out-of-control situations.&nbsp;</li><li>Notifies a supervisor whenever results of assays on QC materials are out-of-range.</li><li>Completes analysis of proficiency testing material within stated turn-around-time.</li></ol></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>Perform additional duties, projects, and/or special assignments when requested.</p><ol style=\"padding-left: 48px;\"><li>Initiates Laboratory Problem Reports or Incident Reports&nbsp;to document complaints, errors, injuries and/or variances from standard procedure.&nbsp;</li><li><p>Perform special projects such as validation, Audits, Quality Indicators and other data as instructed by the supervisor within the agreed upon time period.</p><p>&nbsp;</p></li><li><p>Provide and maintain statistics, as instructed by the supervisor</p><p>&nbsp;</p></li></ol></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt dotted windowtext; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">100%</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\">&nbsp;</td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\">&nbsp;</td></tr></tbody></table></figure>",
    "InternalResponsibilitiesStr": "<p style=\"break-after: avoid;\"><span style=\"font-size: 12pt;\"><strong>Key Responsibilities</strong></span><strong>&nbsp;</strong></p><figure class=\"table\"><table border=\"0\" cellspacing=\"0\" cellpadding=\"0\" width=\"655\" style=\"border-collapse: collapse; width: 491.4pt;\"><tbody><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">%&nbsp;</p><p style=\"text-align: center;\">of time</p></td><td width=\"71\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Essential Function (Yes/No)</p></td><td width=\"501\" valign=\"top\" style=\"border: 1pt solid windowtext; padding: 0in 5.4pt; width: 376.05pt;\"><p style=\"text-align: center;\">&nbsp;&nbsp;</p><p style=\"text-align: center;\">Key Responsibilities</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">50</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>To perform procedures related to cellular therapy processing</p><ol style=\"padding-left: 48px;\"><li>Performs all procedures assigned to the shift in an accurate and efficient manner.</li><li>Learns and performs any new procedure within a reasonable time frame.</li><li><p>Performs procedures in a manner, which does not deviate from the step-by-step procedure write-up. Any deviation from the procedure must be reviewed with a supervisor prior to sending any results.</p><p>&nbsp;</p></li><li>Be responsible for procedural updates by reviewing procedures on an annual basis, checking posted and emailed updates, and by reading and initialing all meeting notes.&nbsp;</li><li><p>Completes test procedures and transmits results in the laboratory computer system within established turn-around times (TATs).</p><p>&nbsp;</p></li><li>Reviews results and validates on computer screen before releasing the results to the LIS (Laboratory Information System).</li><li>Never alters patient test results in any way after they have been released to the LIS except through accepted procedure with documentation.&nbsp;</li><li>Labels specimens, reagents and worksheets with required information in a legible and neat manner with ink pen.</li><li>Completes required training and competency assessments within the assigned time frames.&nbsp;</li><li>Maintains a clean and neat work area. Replenish supplies and prepare reagents as needed.</li><li>Wears buttoned lab coat, gloves and uses face protection when handling patient samples. Exercises proper care and precautions to protect oneself from health hazards. Refrains from smoking, drinking, or eating in and around work areas.</li><li>Take full responsibility for errors when committed, notifies required personnel and completes appropriate documentation.&nbsp;</li><li>Integrates assigned tasks in order to complete the assignments by the end of the work shift.</li><li>Works well without close or continual supervision.</li><li><p>Accepts a reasonable increase in the workload when necessary or assigned by a supervisor.</p><p>&nbsp;</p></li><li>Adheres to all policies and procedures established in the Clinical Laboratory Personnel Policies.</li></ol><p>&nbsp;</p><ol start=\"17\" style=\"padding-left: 48px;\"><li><p>Performs special studies or projects when added to routine procedure run or when assigned separately.</p><p>&nbsp;</p></li><li><p>Process, cryopreserve and distribute all types of cellular therapy products</p><p>&nbsp;</p></li><li><p>Perform sterility cultures and dispense specimens to appropriate locations. Follow-up results of sterility and document in the appropriate worksheet.</p><p>&nbsp;</p></li><li><p>Verify the physician’s order for transplant and coordinate thaw time with the physician or nurse practitioner.&nbsp;</p><p>&nbsp;</p></li><li><p>Review donor eligibility determination before the collection day. Follow-up with the nurse coordinator any missing information and report to the supervisor or designee any problem with donor eligibility.</p><p>&nbsp;</p></li><li><p>Recognize and solve problems, exercising sound judgment to ensure optimal recovery of the cellular therapy products.</p><p>&nbsp;</p></li><li><p>Thaw the cellular therapy products following the thawing procedure.&nbsp;</p><p>&nbsp;</p></li><li>Receive and transport cellular therapy products accurately by following the existing procedure for shipping and receiving including following the National Marrow Donor Program.</li><li>Perform nucleated cell count using automated cell counter.</li><li>Perform CD34, CD3 and 7AAD analysis for cellular therapy products (as applicable). Gate and Analyze the CD34/CD3 population using the Flow analyzer.&nbsp;</li></ol><p>&nbsp;</p></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">35</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>To assist in and ensure smooth operation of the&nbsp;BMT Lab operation</p><ol style=\"padding-left: 96px;\"><li><p>Keep all equipment and other supplies clean, organized, and in proper order in the BMT laboratory. Maintain adequate inventory levels of supplies. Notify the supervisor of any short supply, short dated, or outdated supplies.</p><p>&nbsp;</p></li><li>Maintain equipment in good working order, including adequate liquid nitrogen levels in storage tanks. Perform alarm quality control on all the storage tanks according to schedule.</li><li>Monitor and maintain records for quality control of techniques, reagents, tests and equipment.</li><li>Maintain computer data entry and retrieval system, including engraftment data, bone marrow and aliquot sample inventory, and patient inventory.</li><li>Accurately discard or issue for research cellular therapy products that have been signed off to be discarded by the attending physician.</li><li>Ensure that patients are appropriately flagged in the Clinical Lab computer with regards to need for irradiated blood products, and products having specific blood types.</li><li>Teach residents, fellows and CLS students about ACTL procedures</li><li>To act as lab liaison with Bone Marrow Transplant team and with the nursing units.</li><li>Attend the Adult Bone Marrow Conference Meeting as scheduled by the supervisor.&nbsp;</li><li>Appropriately and accurately write the patients transplant and&nbsp; &nbsp;collections schedule date on the calendar.</li><li><p>Follows cGMP (current Good Manufacturing Practices) in all procedures and in record keeping.</p><p>&nbsp;</p></li></ol></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">10</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>Analyze designated quality control material with all procedures</p><ol><li>Analyzes required quality control material for all procedures.&nbsp;</li><li>Records QC results on worksheet and/or in the LIS.</li><li>Repeats test run if controls are outside the posted control range. Initiate troubleshooting of out-of-control situations.&nbsp;</li><li>Notifies a supervisor whenever results of assays on QC materials are out-of-range.</li><li>Completes analysis of proficiency testing material within stated turn-around-time.</li></ol></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext; border-style: none dotted solid; border-width: medium 1pt 1pt; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">5</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\"><p style=\"text-align: center;\">Yes</p></td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\"><p>Perform additional duties, projects, and/or special assignments when requested.</p><ol style=\"padding-left: 48px;\"><li>Initiates Laboratory Problem Reports or Incident Reports&nbsp;to document complaints, errors, injuries and/or variances from standard procedure.&nbsp;</li><li><p>Perform special projects such as validation, Audits, Quality Indicators and other data as instructed by the supervisor within the agreed upon time period.</p><p>&nbsp;</p></li><li><p>Provide and maintain statistics, as instructed by the supervisor</p><p>&nbsp;</p></li></ol></td></tr><tr><td width=\"83\" valign=\"top\" style=\"border: 1pt dotted windowtext; padding: 0in 5.4pt; width: 62.35pt;\"><p style=\"text-align: center;\">100%</p></td><td width=\"71\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 53pt;\">&nbsp;</td><td width=\"501\" valign=\"top\" style=\"border-color: currentcolor windowtext windowtext currentcolor; border-style: none dotted dotted none; border-width: medium 1pt 1pt medium; padding: 0in 5.4pt; width: 376.05pt;\">&nbsp;</td></tr></tbody></table></figure>",
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