Biospecimen Management Associate I (MN, Tue-Sat)
Guardant Health
Summary
The Biospecimen Associate I supports the management of patient samples and provides the link between the Clinical Operations and Client Services teams. The Biospecimen Associate I is responsible for receiving, unpacking, processing, and recording samples sent for laboratory testing under the supervision of the Biospecimen Management Supervisor.
Job description
The schedule for this position is Midnight shift, Tuesday through Saturday, from 10:00 p.m. to 6:30 a.m. In addition to the primary role of biospecimen management, there may be a need to provide back-up support (non-testing) to the Analytical and/or Post-Analytical team.
Essential Duties and Responsibilities
- Support the laboratory staff with sample intake, accessioning, and processing of all incoming blood specimens.
- Responsible for entering and verifying data in the Laboratory Information Management System (LIMS) database.
- Basic understanding of products (G360, CDx, G360, Reveal, Molecular Response, etc.)
- Prepare samples for testing by isolating plasma from whole blood.
- Ability to prepare and document sample transfers to Clinical Operations department for testing.
- Manage storage of plasma aliquots and blood specimens
- Escalate or resolve and document any discrepancies, or incomplete, and/or unacceptable specimens.
- Operate, maintain, and troubleshoot equipment according to the laboratory's Standard Operating Procedures (SOPs).
- Assist in the organization and upkeep of the laboratory area (daily and weekly maintenance).
- Basic troubleshooting in LIMS and initiating tickets.
- Work closely with the Analytical, Post-Analytical, and Client Services teams to provide consistent and ongoing support to the entire service department.
- Basic understanding of the Nonconforming Event Reports (NCRs), Corrective and Preventative Actions (CAPAs), Analytical Measurement Range (AMR), and Proficiency Testing.
- Communicate test system deviations from the laboratory's established performance specifications by reporting Nonconforming Event Reports (NCRs).
- May assist with internal audits
- May assist with training of new laboratory personnel and training of new procedures with existing personnel.
- Report all concerns of test quality and/or safety to the Supervisor or Safety Officer
- Perform other miscellaneous duties as assigned and assist others as time allows to ensure minimal impact to delivery of results.
Qualifications
- Minimum of Associate of Arts or equivalent experience required.
- Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field preferred
- 0-12 months of laboratory work experience preferred.
- Ability to proactively communicate consistently, clearly, and honestly.
- Strong computing skills
- Demonstrates initiative and good judgment in daily tasks.
- Ability to prepare and maintain records and logs.
- Ability to follow instructions and adhere to standard operating procedures.
- Ability to integrate and apply feedback in a professional manner.
- Ability to prioritize tasks with a high emphasis on quality.
- Solution oriented with ability to escalate issues or problems in a timely manner.
- Ability to work independently and as part of a team.
- AI & Digital Fluency: Demonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the efficiency, effectiveness, and quality of work.
Requirements
- Minimum of Associate of Arts or equivalent experience required
- Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field preferred
- 0-12 months of laboratory work experience preferred
- Strong computing skills
- Ability to prepare and maintain records and logs
- Ability to follow instructions and adhere to standard operating procedures
- Ability to prioritize tasks with a high emphasis on quality
- Ability to work independently and as part of a team
- Ability to proactively communicate consistently, clearly, and honestly
- Demonstrates initiative and good judgment in daily tasks
- Ability to integrate and apply feedback in a professional manner
- Solution oriented with ability to escalate issues or problems in a timely manner
- AI & Digital Fluency
Benefits
- Hybrid Work Model
- Medical, Dental & Vision
- 401(k)
- Paid Time Off
Company overview
Guardant Health, Inc. is a leading precision oncology company headquartered in Palo Alto, California, focused on transforming cancer care through advanced blood and tissue testing technologies. Founded in 2012 by Helmy Eltoukhy and AmirAli Talasaz, who serve as co-CEOs, the company specializes in liquid biopsy tests that detect cancer from circulating tumor DNA in blood samples. Guardant Health's flagship product, Guardant360, was the first comprehensive liquid biopsy test approved by the FDA for tumor mutation profiling and companion diagnostics in non-small cell lung cancer. The company has expanded its portfolio to include Guardant Reveal for residual disease monitoring, Guardant360 TissueNext tissue testing, and Shield, the first FDA-approved blood test for colorectal cancer screening. Guardant Health operates globally with approximately 1,999 employees and generates revenue from precision oncology testing services for clinical and biopharmaceutical customers, as well as development services and technology licensing. The company's innovative approach enables earlier cancer detection, treatment selection, and monitoring, helping to improve patient outcomes across all stages of cancer care.