Biospecimen Associate (4x10 Wednesday-Saturday 830am-700pm)

Company Description

Guardant Health is a leading precision oncology company focused on guarding wellness and giving every person more time free from cancer. Founded in 2012 Guardant is transforming patient care and accelerating new cancer therapies by providing critical insights into what drives disease through its advanced blood and tissue tests real-world data and AI analytics. Guardant tests help improve outcomes across all stages of care including screening to find cancer early monitoring for recurrence in early-stage cancer and treatment selection for patients with advanced cancer. For more information visitand follow the company onLinkedInX (Twitter)andFacebook.

Profile 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. The Biospecimen Associate I has demonstrated an understanding of laboratory workflow.

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. It is imperative that the Biospecimen Associate has demonstrated the ability to work independently but also functions effectively as a member of the Guardant Health team. The nature of the work requires keeping organized records excellent attention to detail effective written and verbal communication skills the ability to multi-task and be flexible with tasks and schedules and the ability to work independently in a team environment.

We are excited to announce that our Biospecimen Management Team has transitioned to a 4-day 10-hour work schedule. We encourage applicants to apply only if this schedule aligns with your availability and preferences.

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.
• 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 laboratorys Standard Operating Procedures (SOPs).
• Assist in the organization and upkeep of the laboratory area (daily and weekly maintenance).
• Work closely with the Analytical Post-Analytical and Client Services teams to provide consistent and ongoing support to the entire service department.
• Communicate test system deviations from the laboratorys established performance specifications by reporting Nonconforming Event Reports (NCRs).
• 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 1-2 years of laboratory work experience preferred.
• Ability to proactively communicate consistently clearly and honestly. Strong computing skills
• Ability to prepare and maintain records and logs.
• 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.

Hybrid Work Model: This section is applicable to onsite employees who are eligible for hybrid work location as specified by management and related policies. Guardant has defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. All U.S. employees who live within 50 miles of a Guardant facility will be required to be onsite on Mondays Tuesdays and Thursdays. We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires. At Guardant our work model has created flexibility for better work-life balance while keeping teams connected to advance our science for our patients.