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Kite Pharma

Develops engineered T cell cancer therapies

Research Associate - Cell Biology, Biomarker Operations

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSanta Monica, CA, USA

About the Job

Requirements

  • High school degree and 3 years of relevant experience, or an associate degree and 2 years of relevant experience, or a bachelor's degree.
  • Experience supporting Multiple Myeloma, hematologic malignancy, cell therapy, or immuno-oncology clinical programs is preferred.
  • Experience managing bone marrow aspirate and biopsy samples is preferred.
  • Experience managing PBMC, serum, plasma, cfDNA, tissue, and other biomarker sample types is preferred.
  • Experience working with central laboratories, specialty testing vendors, and biorepositories is preferred.
  • Familiarity with GCP, GCLP, Laboratory Information Management Systems, and clinical trial operational processes, including biospecimen tracking and inventory management, is preferred.
  • Advanced proficiency with Excel, sample tracking systems, and operational reporting tools is preferred.
  • Experience using AI-enabled productivity, analytics, or project management platforms such as Microsoft Copilot, Power BI, Smartsheet, Jira, Monday.com, or similar tools is preferred.
  • A bachelor's degree in biology, molecular biology, immunology, biotechnology, clinical laboratory science, or a related scientific discipline is preferred.
  • One to four years of experience in clinical research, biomarker operations, laboratory operations, biospecimen management, or a related field is preferred.
  • Experience supporting oncology clinical studies is preferred.
  • Familiarity with Multiple Myeloma clinical research and associated specimen types, including bone marrow and peripheral blood samples, is preferred.
  • Knowledge of biospecimen handling, processing, shipment, and laboratory testing workflows is preferred.
  • Strong organizational skills and attention to detail.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Strong verbal, written, and interpersonal communication skills.
  • Strong project coordination and organizational skills.
  • Attention to detail and data accuracy.
  • Proactive problem-solving skills.
  • Cross-functional collaboration and stakeholder management skills.
  • Vendor management and communication skills.
  • Ability to work independently while managing competing priorities.
  • Digital and AI fluency, with an interest in process improvement and operational innovation.

Responsibilities

  • Support end-to-end biospecimen operations for global oncology clinical trials.
  • Track specimen collection, processing, shipment, receipt, testing, and storage activities.
  • Reconcile sample inventories and support resolution of sample-related queries and discrepancies.
  • Monitor sample shipments and coordinate issue resolution with sites, laboratories, and vendors.
  • Maintain specimen tracking databases and study-specific sample management tools.
  • Ensure accurate documentation and chain-of-custody records throughout the study lifecycle.
  • Assist with the development and review of laboratory manuals, collection guidelines, and sample handling instructions.
  • Review protocols and Schedules of Assessments to identify biomarker collection and testing requirements.
  • Participate in study startup activities, including laboratory vendor setup, sample logistics planning, and site training support.
  • Contribute to study team meetings and biomarker operational discussions.
  • Support implementation of biomarker strategies and sample management plans across multiple studies.
  • Serve as an operational point of contact for central laboratories, specialty testing laboratories, and biorepositories.
  • Coordinate sample transfers and testing requests with vendors.
  • Track laboratory deliverables, sample status, and turnaround timelines.
  • Identify, communicate, and escalate operational risks and issues in a timely manner.
  • Collaborate with vendors to ensure compliance with study requirements and timelines.
  • Support biomarker data reconciliation activities.
  • Maintain study documentation, sample transfer records, operational trackers, and status reports.
  • Assist with generation of sample metrics, dashboards, and study updates.
  • Ensure documentation complies with standard operating procedures, Good Clinical Practice requirements, and applicable regulatory standards.
  • Use AI-powered tools and digital solutions to support study planning, sample tracking, vendor oversight, and operational reporting.
  • Use automation and data-driven insights to improve biomarker workflow efficiency and proactively identify operational risks.
  • Develop and maintain dashboards, metrics, and performance reports to support clinical trial execution and decision-making.
  • Contribute to continuous improvement initiatives through adoption of AI and digital technologies.
  • Use Microsoft Copilot, advanced analytics platforms, workflow automation solutions, and data visualization technologies to streamline routine tasks, increase operational efficiency, improve data quality, identify risks proactively, and accelerate decision-making across biomarker programs.

Desired Qualifications

  • Experience supporting Multiple Myeloma, hematologic malignancy, cell therapy, or immuno-oncology clinical programs.
  • Experience managing bone marrow aspirate and biopsy samples.
  • Experience managing PBMC, serum, plasma, cfDNA, tissue, and other biomarker sample types.
  • Experience working with central laboratories, specialty testing vendors, and biorepositories.
  • Familiarity with GCP, GCLP, Laboratory Information Management Systems, and clinical trial operational processes, including biospecimen tracking and inventory management.
  • Advanced proficiency with Excel, sample tracking systems, and operational reporting tools.
  • Experience using AI-enabled productivity, analytics, or project management platforms such as Microsoft Copilot, Power BI, Smartsheet, Jira, Monday.com, or similar tools.
  • A bachelor's degree in biology, molecular biology, immunology, biotechnology, clinical laboratory science, or a related scientific discipline.
  • One to four years of experience in clinical research, biomarker operations, laboratory operations, biospecimen management, or a related field.
  • Experience supporting oncology clinical studies.
  • Familiarity with Multiple Myeloma clinical research and associated specimen types, including bone marrow and peripheral blood samples.
  • Knowledge of biospecimen handling, processing, shipment, and laboratory testing workflows.

About the Company

Kite Pharma

Develops engineered T cell cancer therapies

Kite Pharma develops cancer immunotherapies by engineering a patient’s own T cells to attack tumors. Its core product strategy centers on cell therapy where T cells are genetically modified to recognize cancer cells, expanded outside the body, and then infused back into the patient to destroy cancer. This approach differs from traditional drugs by using the immune system itself to fight cancer and by tailoring therapies to individual patients. Kite focuses on clinical trials and commercialization of approved therapies, often through partnerships and licensing with other pharmaceutical companies to reach patients worldwide. The company’s goal is to provide potentially lifesaving, durable cancer treatments and move toward a cure for cancer.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Santa Monica, CA
Founded
2009

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