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Featured Employers
Senior Clinical Research Associate
Company: Guardant Health
Location: Redwood City, CA
Employment Type: Full Time
Date Posted: 06/25/2022
Expire Date: 08/22/2022
Job Categories: Biotechnology and Pharmaceutical, Computers, Software, Healthcare, Other, Healthcare, Practitioner and Technician, Information Technology, Research & Development, Medical
Job Description
Senior Clinical Research Associate

Company Description

Guardant Health is a leading precision oncology company focused on helping conquer cancer globally through use of its proprietary blood 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 launched liquid biopsy-based Guardant360®, Guardant360 CDx and GuardantOMNI® tests for advanced stage cancer patients. These tests fuel development of its LUNAR program, which aims to address the needs of early stage cancer patients with neoadjuvant and adjuvant treatment selection, cancer survivors with surveillance, asymptomatic individuals eligible for cancer screening and individuals at a higher risk for developing cancer with early detection.

Job Description

The Senior Clinical Research Associate (CRA) is responsible for management and monitoring activities that will lead to successful execution of clinical studies. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The 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.
  • Involvement in the generation of project plans, especially those related to site management, monitoring and reporting.
  • Involved in the development of protocols and Case Report Forms (CRFs) as assigned.
  • Manage the identification, selection and feasibility processes.
  • 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 the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review and monitor for missing or implausible data.
  • Prepare accurate and timely trip 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.

Qualifications

  • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing, medical or laboratory technology.
  • Minimum of five + (5) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) at a Pharmaceutical, Biotech or CRO company. Diagnostic and/or Medical device experience preferred.
  • Oncology experience preferred.
  • 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 70% of the time.
  • Excellent knowledge of MS Office as well as project management and clinical trials software.

Additional Information

Covid Vaccination Policy:  Starting January 7, 2022, Guardant Health will require all employees to be fully vaccinated to either (a) establish that they have been fully vaccinated against COVID-19; or (b) request and obtain an approved exemption from Guardant’s COVID-19 U.S. Vaccination Policy as a reasonable accommodation, as consistent with applicable laws.  An employee is considered fully vaccinated against COVID-19 two weeks after receiving the second dose of a two-dose vaccine or one dose of a single-dose vaccination. Acceptable vaccines are approved or under emergency use authorization by the U.S. Food and Drug Administration (FDA) and/or the World Health Organization (WHO). In addition, fully-vaccinated employees will be required to maintain their fully-vaccinated status under this policy by obtaining, if applicable, any FDA-approved boosters.

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 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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Company Name: Guardant Health
Website: https://www.smartrecruiters.com/Gua...
Company Description:

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