Clinical Trial Assistant

  • Location
    Irvine , California
  • Category
    Medical & Science - Pharmaceutical - Clinical
  • Job type

A Clinical Trial Assistant job in Irvine, CA is available through Adecco Medical and Science. You must have at least one-year experience in a pharmaceutical or industry or CRO. You will be responsible for supporting the Clinical Trial Management/operational study team to manage the various aspects of the operational execution and delivery of quality studies.

Clinical Trial Assistant job responsibilities include:
• Responsible for operations and procedural support on contracting, vendor set-up, purchase requisitions, and payments processing.
• Responsible for generating and maintaining periodic reporting requirements including but not limited to Transfer of Value reporting (e.g. Sunshine Act), monthly reports to Brands R&D, monthly global study reports to Pharmacovigilance, and quarterly reports to support Pharmacovigilance submissions.
• Works directly with project managers (e.g. Study Managers, Publication Managers, etc.) to ensure all requirements are completed for proper onboarding of vendors.
• Consult and coordinate as necessary with stakeholders to understand latest business policies or processes and identify potential impact to current processes.

• Associate degree or higher preferred
• One to two years relevant experience in pharmaceutical industry or CRO
• Experience supporting clinical trials
• Basic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plus

If you are interested in this Clinical Trial Assistant job in Irvine, CA then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to If you have questions about the position or would like more information, please contact Stephanie Pack by email at
Equal Opportunity Employer Minorities/Women/Veterans/Disabled

  • Apply with Adecco

Reference number US_EN_2_108175_318434