Shalini Pereira Email & Phone Number
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Shalini Pereira is listed as Director, Clinical Consultant, Accreditation, Regulatory, Compliance, CLIA Certified at Tempus AI, a with 23 employees, based in Seattle, Washington, United States. AeroLeads shows a matched LinkedIn profile for Shalini Pereira.
Shalini Pereira previously worked as Director, Clinical Consultant, Accreditation, Regulatory, Compliance, CLIA Certified at Sengine Precision Medicine and Director, Clinical Consultant, Accreditation, Regulatory, Compliance at Scisco Genetics Inc. Shalini Pereira holds Doctor Of Philosophy (Phd), Biochemistry from University Of Rochester.
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About Shalini Pereira
I am a Clinical/ Healthcare/ Academic Leader, Clinical Laboratory Director and Clinical Consultant with extensive experience in Histocompatibility and Immunogenetics, Transplant Immunology, Diagnostic Immunology, Clinical Chemistry and Serological and Molecular technologies.I am CLIA certified and Board-certified for high-complexity Clinical laboratory management, by the American Board of Histocompatibility and Immunogenetics (ABHI).I have been responsible for quality and compliance management, strategic planning, budget management, oversight of staff, developing and validating new testing technologies and platforms and consulting with clinical programs where specialized testing/interpretation is required, . Specialties: Operations, Strategic Planning, Team Leadership, Budgets, Teaching, Compliance, Regulatory, Accreditation, Quality Assurance and Quality Monitoring, Lab Test Utilization Management, High Complexity Clinical Laboratories, Histocompatibility, Solid Organ Transplantation, Bone marrow/ Hematopoietic stem cell Transplantation, Transfusion Support, Immunology, Molecular Biology, Cancer, Next Generation Sequencing, Molecular Diagnostics, Biochemistry,
Listed skills include Immunology, Molecular Biology, Genetics, Pcr, and 35 others.
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Shalini Pereira work experience
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Director, Clinical Consultant, Accreditation, Regulatory, Compliance, Clia Certified
Current
Director, Clinical Consultant, Accreditation, Regulatory, Compliance
CurrentEstablished in 2006, Scisco Genetics Inc. is accredited by the American Society for Histocompatibility and Immunogenetics (ASHI), the Clinical Laboratory Improvement Amendments (CLIA) program, and the Washington State Department of Health. Fast and accurate high resolution genotyping of complex immune regions is critical to improving transplant outcomes and understanding disease associations.Scisco Genetics is dedicated to:• Providing high quality sequence-based typing solutions and services for complex immune gene systems, including HLA and KIR.• Enabling Next Generation Sequencing technology in clinical laboratories that support transplant programs.• Continuous quality improvement in sequencing technology and software analysis tools.Key Responsibilities include:• Clinical Guidelines development• Technical Services and Accreditation• Quality and Compliance - Maintaining quality control and quality assessment programs, ensuring, resolving technical problems, ensuring corrective action when test systems deviate from established performance • Evaluation of new equipment and tests - validation of new testing technologies and platforms, determining acceptable levels of analytical test performance• The competency of laboratory personnel, including participation in proficiency testing programs, training in methodologies, and continuing education.
Director, Technical And Admin, Operations, Quality, Compliance, Accreditation, Utilization Mgment
Founded in 1947, Group Health Cooperative is a consumer-governed, nonprofit health care system that coordinates care and coverage. Based in Seattle, Wash., Group Health and its subsidiary health carriers, Group Health Options, Inc. and KPS Health Plans, serve more than half a million residents of Washington state and IdahoAppointed to be responsible for technical and clinical services, overall laboratory quality, and compliance performance within the internal and external delivery system. To leverage the technical expertise of a team of pathologists, other practitioners and industry colleagues to lead the design, development, and implementation of department strategies, and work with business operations leaders to manage strategies deployments. Group Health has 22 laboratory locations in Washington. Key responsibilities included:• Test Utilization Management, • Clinical Guidelines development,• Technical Services • Quality and Compliance• Evaluation of new equipment and tests • Business owner of the Laboratory Information System (LIS)
Director, Clinical Consultant, Operations, Accreditation, Regulatory, Compliance, Clia Certified
The clinical laboratory supports physicians, scientists and clinical staff involved in treatment and research for patients with cancer at the FHCRC; the Center is known for its pioneering work in bone marrow transplantation. “The Hutch” is a not-for-profit teaching and scientific research center, working with patients and supporting research aimed at improving treatment outcomes for people with cancer or with critical organ failure.I was responsible for overall operation and administration of the Clinical Immunogenetics laboratory, including technical and scientific oversight, training of personnel, accuracy of testing, reporting, and regulatory compliance. My responsibilities included: • Selecting test methodologies, development and validation of new testing technologies and platforms, determining acceptable levels of analytical test performance, development and validation of standard processes for workflow in the laboratory, and between the laboratory and stakeholders• Maintaining quality control and quality assessment programs, ensuring, resolving technical problems, ensuring corrective action when test systems deviate from established performance • Providing advice in support of donor search and selection processes and ensuring that consultation is available to the laboratory's clients relating to the quality of test results and their interpretation• The competency of laboratory personnel, including participation in proficiency testing programs, training in methodologies, and continuing education.• Interactions with stakeholder clinical programs and services
Assistant Director, Clinical Consultant, Accreditation, Quality, Compliance, Technical
The Stanford Histocompatibility Laboratory supports the Histocompatibility, Immunogenetics and Disease Profiling testing needs of all transplant programs at the Stanford Medical Center and at the Lucille Packard Children’s Hospital at Stanford, including liver, kidney, pancreas, heart, lung, small bowel and human stem cell (HSC/BMT) transplantation. The transplant programs at Stanford Hospital & Clinics have earned a number of distinctions including performing the first adult heart transplant in the US, the first heart-lung transplant in the world and have outstanding outcomes for both patient and graft survival, The Bone Marrow Transplant program at Stanford performs auto and allo transplantations for approximately 200 adult patients/year. My responsibilities included:• Involvement in all aspects of the performance of clinical tests and interpretation of results • Providing first call for assay results where technologists had difficulty interpreting the data• Identifying individual problems and defining strategies for resolution• Conveying relevant information to clinicians • Providing consultations to physicians for platelet transfusion support and advice on the use of compatible donors• Providing literature reviews • Delivering lectures on transplantation for Clinical training at various Bay Area Hospitals.• Coordinating didactic and clinical rotations for Residents and Fellows
Trainee Director, Immunogenetics And Transplantation Laboratory
The Immunogenetics and Transplantation Laboratory (ITL) provides specialized diagnostic services for allogeneic transplantation and conducts related research. The laboratory provides support for blood, bone marrow, kidney, pancreas, liver, heart, lung, small bowel, and cornea transplantation. UCSF has performed more kidney transplants than any other hospital in the world. About 1,200 patients/ year are evaluated as potential transplant candidates with more than 300 kidney transplants performed/year. The ITL is a national reference laboratory, a referee laboratory for the ASHI proficiency testing program, a NMDP contract laboratory, a core laboratory for the NIH Immune Tolerance Network, and a participant in several national clinical trials. The laboratory also conducts basic research and provides educational programs for health care professionals. The laboratory is not-for-profit and is owned and operated by the University of California, San Francisco.Laboratory and Clinical Experience:• Provided consultations on sensitization and screening histories, as well as the cross-match results of high risk solid organ (live donor) transplant candidates • Modified a lab procedure utilizing pronase treated lymphocytes in flow cytometry • Developed Quality Assurance/ Quality Monitoring (QA/ QM) monitoring forms for compliance with CLIA, CA state and ASHI regulations • Performed monthly and quarterly monitoring of QA/QM indicators • Observed trends and evaluated the effectiveness of corrective actions • Served on a subcommittee for compliance with the National Society Standards and updates to CLIA regulations codified in 2004 • Served on the National Society’s Quality Assurance/ Standards Committee that reviews and updates Quality Assurance/ Standards
Researcher, Post - Doctoral Fellow
Laboratory Experience:• Characterization of the gene disrupted in the Roi mutation in D. melanogaster • Characterized the roles played by the Src-family kinases in signaling and effector functions in immune cells. • Provided the first evidence that resting murine neutrophils express on their surface a novel integrin (alpha4). • First demonstrated that the Src kinase Lyn plays an inhibitory role in integrin and cytokine signaling in myeloid cells • First demonstrated that the ITIM-containing receptor PIR-B is involved in inhibiting downstream integrin and cytokine signaling in myeloid cells • Mapped the appropriate regions of the mouse Lyn and Fgr genes and constructed vectors for the targeted insertion of kinase-inactive and floxed mutant alleles in embryonic stem cells.• Investigated the role of Faf1 (fas-associated factor 1) in autoimmune disease. Activities: Served on the steering committee of ‘Women in Life Sciences’ (WILS) 2001-2003a UCSF women run organization, which serves as a networking and support structure for UCSF women scientists at all levels of their career
Shalini Pereira education
Doctor Of Philosophy (Phd), Biochemistry
Master Of Science (Ms), Biochemistry
B.S., Microbiology And Biochemistry
Frequently asked questions about Shalini Pereira
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What company does Shalini Pereira work for?
Shalini Pereira works for Tempus AI.
What is Shalini Pereira's role at Tempus AI?
Shalini Pereira is listed as Director, Clinical Consultant, Accreditation, Regulatory, Compliance, CLIA Certified at Tempus AI.
Where is Shalini Pereira based?
Shalini Pereira is based in Seattle, Washington, United States while working with Tempus AI.
What companies has Shalini Pereira worked for?
Shalini Pereira has worked for Tempus Ai, Sengine Precision Medicine, Scisco Genetics Inc, Group Health Cooperative, and Fred Hutchinson Cancer Research Center And The University Of Washington, Seattle.
Who are Shalini Pereira's colleagues at Tempus AI?
Shalini Pereira's colleagues at Tempus AI include Lauren Appleyard.
How can I contact Shalini Pereira?
You can use AeroLeads to view verified contact signals for Shalini Pereira at Tempus AI, including work email, phone, and LinkedIn data when available.
What schools did Shalini Pereira attend?
Shalini Pereira holds Doctor Of Philosophy (Phd), Biochemistry from University Of Rochester.
What skills is Shalini Pereira known for?
Shalini Pereira is listed with skills including Immunology, Molecular Biology, Genetics, Pcr, Transplant, Life Sciences, Cancer, and Flow Cytometry.
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