Clinical Research Gastroenterologist (Part-time) - Long Beach, CA

Protouch Staffing

Long Beach, CAFull-timePosted Apr 1, 2026

Behavioral Health Market Context

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Benefits

Health Insurance

Job Description

ibility.
• Ensure patient safety, monitor adverse events (AEs/SAEs), and oversee treatment outcomes.
• Review and approve study-related documentation in compliance with study protocols and regulatory standards.
• Collaborate with study coordinators, nurses, and research staff to ensure accurate documentation and protocol adherence.
• Participate in protocol training and maintain compliance with Good Clinical Practice (GCP) and FDA regulations.

Qualifications:
• M.D. or D.O. with an active, unrestricted California medical license.
• Board-certified in Gastroenterology .
• Prior clinical research experience preferred (training available).
• Strong organizational, communication, and teamwork skills.
• Valid DEA license and current BLS/ACLS certification (preferred).

Compensation & Benefits:
• Competitive hourly rate: $100 - $200/hour (based on specialty and experience).
• Highly flexible, supplemental schedule (ideal for additional income or work-life balance).
• Opportunity to gain or expand experience in clinical research.
• Contribute to advancing medical innovation and patient care.

Qualifications

  • Start Date: Within 0-6 months
  • M.D. or D.O. with an active, unrestricted California medical license
  • Board-certified in Gastroenterology
  • Strong organizational, communication, and teamwork skills

Benefits

  • Competitive hourly rate: $100 - $200/hour (based on specialty and experience)
  • Highly flexible, supplemental schedule (ideal for additional income or work-life balance)
  • Opportunity to gain or expand experience in clinical research
  • Contribute to advancing medical innovation and patient care

Responsibilities

  • Job Type: Part-time (0-8 hours per week, flexible schedule)
  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on assigned Gastroenterology clinical trials
  • Conduct participant evaluations, specialty assessments, and medical examinations to determine study eligibility
  • Ensure patient safety, monitor adverse events (AEs/SAEs), and oversee treatment outcomes
  • Review and approve study-related documentation in compliance with study protocols and regulatory standards
  • Collaborate with study coordinators, nurses, and research staff to ensure accurate documentation and protocol adherence
  • Participate in protocol training and maintain compliance with Good Clinical Practice (GCP) and FDA regulations


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