Guardant Health is a leading precision oncology company focused on helping conquer cancer globally through use of its proprietary tests, vast data sets and advanced analytics. The Guardant Health oncology platform leverages capabilities to drive commercial adoption, improve patient clinical outcomes and lower healthcare costs across all stages of the cancer care continuum. Guardant Health has commercially launched Guardant360®, Guardant360 CDx, Guardant360 TissueNext™, Guardant360 Response™, and GuardantOMNI® tests for advanced stage cancer patients, and Guardant Reveal™ for early-stage cancer patients. The Guardant Health screening portfolio, including the Shield™ test, aims to address the needs of individuals eligible for cancer screening.

The Clinical Study Coordinator is responsible for monitoring and management for clinical studies performed at Guardant Health, and assisting with their set up and close out. The work requires keeping meticulous and organized records, excellent attention to detail, the ability to prioritize, and to be flexible with tasks and schedules.  

Essential Duties and Responsibilities: 

Facilitate the coordination and management of clinical studies 

Prepare records for trial monitoring activities and study binder maintenance 

Host monitoring visits and close out action items in a timely manner 

Identify high complexity problems which adversely affect clinical studies 

Assist with training of new study coordinators 

Assist with developing Standard Operating Procedures or supplemental study material 

Review protocols and procedures for clinical studies and compare with the laboratory’s standard operating procedures 

Document study related nonconformance reports and corrective actions taken when test systems deviate from the laboratory’s established performance specifications for clinical studies 

Assist with process improvement activities for the Clinical Study Coordination team 

Participate in internal and external audit activities, as needed 

Perform other miscellaneous duties as assigned and assist others as time allows 

Report all concerns of test quality and/or safety to the Laboratory Director or Safety Officer 

Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field 

1  year experience in a CLIA, CAP accredited laboratory preferred 

1-2 years of experience as a clinical research coordinator preferred, ideally in a lab or device setting 

Project management experience preferred 

Knowledge of ICH/GCP guidelines, including basic understanding of regulatory requirements in other countries, preferred 

Working knowledge of local, state, and federal laboratory regulations 

Able to integrate and apply feedback in a professional manner 

Able to prioritize and drive to results with a high emphasis on quality 

Proven ability to demonstrate high attention to detail and accuracy 

Able to work effectively in a team environment and build strong working relationships 

Effective interpersonal skills and ability to effectively communicate (verbal and written) across all levels of the company  

Other: Clinical Laboratory certification (MT, ASCP or equivalent) or certification as a clinical research professional (SOCRA, ACRP) is desirable 

Work Environment: 

Employee may be required to lift routine office supplies and use office equipment. Majority of the work is performed in a desk/ office environment. However, there may be exposure to high noise levels, fumes, and biohazard material in the laboratory environment. Ability to sit for extended periods of time. Hours and days may vary depending on operational needs. 

Some lifting (up to 25 pounds) may be necessary 

Hybrid Work Model: At Guardant Health, we have 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.

For positions based in Palo Alto, CA or Redwood City, CA, the base salary range for this full-time position is $80,600 to $108,810. The range does not include benefits, and if applicable, bonus, commission, or equity.

Within the range, individual pay is determined by work location and additional factors, including, but not limited to, job-related skills, experience, and relevant education or training. If you are selected to move forward, the recruiting team will provide details specific to the factors above.

Employee may be required to lift routine office supplies and use office equipment. Majority of the work is performed in a desk/office environment; however, there may be exposure to high noise levels, fumes, and biohazard material in the laboratory environment. Ability to sit for extended periods of time.

Guardant Health is committed to providing reasonable accommodations in our hiring processes for candidates with disabilities, long-term conditions, mental health conditions, or sincerely held religious beliefs. If you need support, please reach out to [email protected]

Guardant Health 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, or protected veteran status and will not be discriminated against on the basis of disability.

All your information will be kept confidential according to EEO guidelines.

To learn more about the information collected when you apply for a position at Guardant Health, Inc. and how it is used, please review our Privacy Notice for Job Applicants.

Please visit our career page at: http://www.guardanthealth.com/jobs/

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