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Psychiatrist (Clinical Trial) - Part Time- Pomona, CA

  • ... Posted on: Mar 19, 2026
  • ... ProTouch Staffing
  • ... Pomona, Missouri
  • ... Salary: Not Available
  • ... Full-time

Psychiatrist (Clinical Trial) - Part Time- Pomona, CA   

Job Title :

Psychiatrist (Clinical Trial) - Part Time- Pomona, CA

Job Type :

Full-time

Job Location :

Pomona Missouri United States

Remote :

No

Jobcon Logo Job Description :

Job Description

Psychiatrist (Clinical Trial) - Part Time- Pomona, CA

Job Type: Part Time

Shifts: 0-8 hours/week

Key Responsibilities:

  • Serve as Sub-Investigator or Principal Investigator in clinical trials.

  • Conduct medical evaluations of participants and assess eligibility.

  • Monitor safety, adverse events, and treatment response throughout the study.

  • Review and sign study-related documentation as required by protocol and regulations.

  • Collaborate with study coordinators, nurses, and research staff.

  • Attend protocol-related training sessions and maintain compliance with Good Clinical Practice (GCP).

Qualifications:

  • MD or DO with an active California medical license.

  • Board-certified in Psychiatry.

  • Interest in clinical research (prior experience preferred but not required-training provided).

  • Strong communication and organizational skills.

Benefits:

  • Flexible scheduling (0-8 hours/week).

  • Professional growth in clinical research.

  • Contribution to advancing medical treatments in psychiatry.


View Full Description

Jobcon Logo Position Details

Posted:

Mar 19, 2026

Reference Number:

ce926075acef3fa0

Employment:

Full-time

Salary:

Not Available

City:

Pomona

Job Origin:

ziprecruiter

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Job Description

Psychiatrist (Clinical Trial) - Part Time- Pomona, CA

Job Type: Part Time

Shifts: 0-8 hours/week

Key Responsibilities:

  • Serve as Sub-Investigator or Principal Investigator in clinical trials.

  • Conduct medical evaluations of participants and assess eligibility.

  • Monitor safety, adverse events, and treatment response throughout the study.

  • Review and sign study-related documentation as required by protocol and regulations.

  • Collaborate with study coordinators, nurses, and research staff.

  • Attend protocol-related training sessions and maintain compliance with Good Clinical Practice (GCP).

Qualifications:

  • MD or DO with an active California medical license.

  • Board-certified in Psychiatry.

  • Interest in clinical research (prior experience preferred but not required-training provided).

  • Strong communication and organizational skills.

Benefits:

  • Flexible scheduling (0-8 hours/week).

  • Professional growth in clinical research.

  • Contribution to advancing medical treatments in psychiatry.


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