Senior Clinical Research Associate

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.

Position Summary:

The Senior Clinical Research Associate (CRA) is responsible for management and monitoring activities that will lead to successful execution of IVD clinical studies.They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The Sr. CRA engages with study investigators, vendors and internal/external stakeholders as a member of the Clinical Trial Operations team.

Essential Duties and Responsibilities:

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits.
• Independently generate project plans, especially those related to site management, monitoring and reporting.
• Mentor and provide guidance to junior monitors on best monitoring practices.
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
• Ensure that study management, data collection and subsequent data transfers are in accordance with outlined specifications (DTA/DTS).
• Independently prepare accurate and timely trip reports.
• Ensure compliance to monitoring plans by scheduling monitoring visits and reviewing and approving monitoring reports.
• Organize and make presentations at Investigator Meetings
• Interact with internal groups to evaluate needs, resources, and timelines.
• Act as contact for clinical trial supplies and other suppliers (vendors) as assigned
• Provide project management support to pharmaceutical partners.
• Thorough understanding of the principles of the assay and/or instrument and "hands-on" knowledge.

• Bachelor's degree in life sciences or a related field with a minimum of 5 years of clinical research monitoring experience (including pre-study, initiation, routine monitoring, and closeout visits) at a Pharmaceutical, Biotech, or CRO company OR
• Master's degree in life sciences or a related field with a minimum of 3 years of clinical research monitoring experience.
• Experience in diagnostics and/or medical devices is preferred.
• Experience with companion diagnostics (CDx) is advantageous
• Oncology experiencepreferred
• Thorough knowledge of ICH/GCP Guidelines, including a basic understanding of regulatory requirements in other countries
• Advanced site monitoring skills
• The ability to thrive with minimal supervision
• The drive to resolve project-related problems and can prioritize workload for self and team
• Efficient and effective work habits in a matrix environment, internally and externally
• A flexible attitude to adjust to changing needs
• The ability and willingness to travel up to 10% of the time
• Excellent knowledge of MS Office as well as project management and clinical trials software

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 $105,600 to $142,560. 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 toPeopleteam@guardanthealth.com

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.

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