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Clinical Research Specialist

Job in Irvine, Orange County, California, 92614, USA
Listing for: TalentBurst, Inc.
Full Time position
Listed on 2026-07-15
Job specializations:
  • Research/Development
    Clinical Research, Medical Science
  • Healthcare
    Clinical Research, Medical Science
Job Description & How to Apply Below

Position: Clinical Research Specialist, Req# 18246-1

This is an in-house CRA Role.
Location:
Irvine, CA (100% onsite)

Duration: 12+ months contract to hire

Job Description:

The main function of a clinical research specialist is to perform study start-up and conduct activities including ICF review that meet regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities.

Education and Experience:

  • Bachelor's Degree or equivalent in a related field
  • 2-4 years of experience required
  • Clinical background, familiar with clinical study process, monitoring, GCP and clinical study relevant regulations.
  • High compliance requirements and understanding that the rights and well-being of human subjects should be protected during a clinical study

Key Responsibilities:

  • Perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities
  • Identify and investigate discrepancies in study documentation by applying clinical protocol and GCP knowledge and develop processes to mitigate reoccurrence throughout study phases
  • Identify and investigate discrepancies in study documentation by applying clinical protocol and GCP knowledge and develop processes to mitigate reoccurrence throughout study phases
  • Conduct in-house and site (if applicable) reviews of associated documentation and participate in internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations
  • Assess current processes, identify opportunities and propose solutions to improve process efficiency within and across related functional areas
  • Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution

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#ZR

Why Talent Burst?
At Talent Burst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth.

Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships.

We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options.

Talent Burst is an equal opportunity employer committed to an inclusive and diverse workforce.

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