Psychiatry Clinical Trial Physician (0-8 hours/week) - Pasadena, CA

Protouch Staffing

Pasadena, CAFull-timePosted Mar 29, 2026

Behavioral Health Market Context

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Job Description

of trials, ensuring patient safety, and maintaining regulatory compliance.

Key Responsibilities include:
• Screen, evaluate, and monitor study participants.
• Ensure adherence to study protocols, FDA, IRB, and GCP standards.
• Accurately document data, adverse events, and outcomes.
• Collaborate closely with coordinators and clinical research staff for smooth trial execution.
Education, Licensure, and Experience:
• MD or DO with an active California medical license.
• Board certification - Psychiatry
• Prior clinical research experience preferred (training available).
• Strong communication, organizational, and teamwork skills.
Benefits:
• Competitive pay: $100-$200/hr (based on specialty and experience).
• Flexible schedule (0-8 hours/week).
• Research training provided for physicians new to clinical trials.
• Opportunity to contribute to medical innovation while continuing private practice.
For more information please reach out to Kuldeep Singh at View phone number on click.appcast.io or View email address on click.appcast.io m

Qualifications

  • MD or DO with an active California medical license
  • Board certification - Psychiatry
  • Strong communication, organizational, and teamwork skills

Benefits

  • Competitive pay: $100-$200/hr (based on specialty and experience)
  • Flexible schedule (0-8 hours/week)
  • Research training provided for physicians new to clinical trials
  • Opportunity to contribute to medical innovation while continuing private practice

Responsibilities

  • Physicians will play a key role in overseeing medical aspects of trials, ensuring patient safety, and maintaining regulatory compliance
  • Screen, evaluate, and monitor study participants
  • Ensure adherence to study protocols, FDA, IRB, and GCP standards
  • Accurately document data, adverse events, and outcomes
  • Collaborate closely with coordinators and clinical research staff for smooth trial execution


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