Clinical Trials Associate – ImmunityBio, Inc
ImmunityBio, Inc., a leading biotechnology company, is seeking a Clinical Trials Associate to join its team in El Segundo, California. The role supports the efficient administration and conduct of clinical research studies, contributing to the companyโs mission of developing immunotherapies that harness the bodyโs natural defense mechanisms to fight cancer and infectious diseases. Openings for Clinical Trial Jobs. Join for the Clinical Research Job as Clinical Research Associate and advance medical innovation.
Clinical Trial Associate Job Details:
- Position: Clinical Trials Associate
- Location: El Segundo, CA (Mariposa)
- Time Type: Full-time
- Job Requisition ID: R2710
- Posted: 22 Days Ago
- Work Type: On-site or remote (depending on location)
- Schedule: Monday โ Friday, standard business hours
- Salary Range:
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National Market: $69,100 โ $76,000 annually
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Premium Market (Los Angeles, San Diego, SF, NYC, Chicago, Boston): $72,800 โ $80,000 annually
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- Additional Benefits: Discretionary bonus and equity award eligibility
About the Company:
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing next-generation cell and immunotherapy products. Their innovative research focuses on reprogramming the immune system to eliminate cancerous or infected cells, providing a lasting immune memory to prevent recurrence. With a vision to transform how diseases like cancer are treated, ImmunityBio is pioneering therapies that amplify the immune response to target disease at its root.
Headquartered in Southern California, ImmunityBio provides a collaborative and growth-oriented environment for professionals passionate about advancing medical innovation.
Educational Requirements for the Clinical Trial Associate role:
- Bachelorโs degree in a scientific or related discipline with 0โ2 years of clinical research experience, OR
- High school diploma with 5+ years of relevant clinical research experience.
Key Responsibilities of the Clinical Trial Associate:
- Support Clinical Operations teams to meet project and departmental goals.
- Maintain and apply knowledge of ICH GCP, regulatory standards, and SOPs.
- Organize and maintain clinical study documentation (e.g., Trial Master File, study-level and site-level documents).
- Review documents for compliance with Good Documentation Practices (GDocP).
- Audit site invoices, reconcile payments, and track IRB submissions.
- Coordinate and facilitate study start-up activities and clinical site communications.
- Prepare agendas, meeting minutes, and assist in team coordination.
- Manage materials, purchase requisitions, and invoice approvals in ERP systems.
- Participate in safety reporting activities and ensure accurate documentation.
- Perform additional projects and duties as required.
Skills Required for the Clinical Trial Associate:
- Proficiency in MS Word, Excel, PowerPoint, Outlook, Adobe.
- Strong organizational, multitasking, and documentation skills.
- Excellent oral and written communication abilities.
- Attention to detail and ability to maintain confidentiality.
- Working knowledge of Good Documentation Practices (GDP).
- Time management and ability to work independently or collaboratively.
How to Apply?
Interested applicants for the Clinical Research Job can apply directly via ImmunityBioโs official careers portal. Candidates interested for the Clinical Research Associate role should ensure their resume highlights experience in clinical research operations and trial administration.
