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Clinical Research Assistant

Los Angeles, Temple City, Full-Time

Summary of Position

The Clinical Research Assistant/Associate will act as the “in-house” clinical and regulatory link to clinical study managers, contract research organizations (CROs), and investigational sites. He or She will assist the execution of the company’s clinical research projects to assure adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures.

Key Responsibilities

  • Assist all clinical research activities from study planning through closure
  • Maintain timely and effective communication between internal study team and external vendors
  • Prepare meeting agendas and summarize meeting minutes
  • Maintain precise records of study documentations, including protocols, amendments, informed consent forms, regulatory forms, drug dispensation records etc.
  • Support evaluation, selection, initiation and auditing of clinical sites
  • Support management of study related work, including drug distribution, clinical sample receiving and storage
  • Support in preparation of data reports, summaries, presentations
  • Support preclinical research if needed

Qualifications

  • BS or MS in life sciences or related degree
  • 2-5 years of relevant experience working in the pharmaceutical/biotechnology industry or CROs
  • Experience in study site selection and auditing
  • Experience in vendor management (CRO and laboratory)

Compensation and Benefits

This is a full-time position. Fulgent Pharma offers a competitive compensation and benefits package which includes but is not limited to salary, health insurance, dental insurance, 401(K) and stock options.


To apply, please email your cover letter and resume to applyjob@fulgentpharma.com.



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