Dermatologist (Clinical Trails) - Part-time - Pasadena, CA

ProTouch Staffing

Pasadena, CAPart-time and Contractor

100–200 an hour

Behavioral Health Market Context

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Job Description

ator (Sub-I) in our current and upcoming clinical trials. The Dermatologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with the research team to maintain high-quality trial execution.

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Key Responsibilities

• Serve as PI or Sub-I in assigned clinical trials.

• Conduct medical evaluations and assess participant eligibility.

• Monitor patient safety, adverse events, and treatment outcomes.

• Review and sign study-related documentation per protocol and regulations.

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

• Attend protocol training and ensure adherence to Good Clinical Practice (GCP).

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Qualifications

• MD or DO with an active California medical license.

• Board-certified in Dermatology.

• Interest in clinical research (prior experience preferred; training provided if needed).

• Strong communication, teamwork, and organizational skills.

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Benefits

• Flexible schedule: 0-8 hours/week.

• Professional growth opportunities in clinical research.

• Contribute to advancing dermatology treatments and patient outcomes.

Qualifications

  • MD or DO with an active California medical license
  • Board-certified in Dermatology
  • Strong communication, teamwork, and organizational skills

Benefits

  • Compensation: $100-$200/hr (based on market standard rates)
  • Flexible schedule: 0-8 hours/week
  • Professional growth opportunities in clinical research
  • Contribute to advancing dermatology treatments and patient outcomes

Responsibilities

  • Start Date: Within 0-6 months
  • We are seeking a board-certified Dermatologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in our current and upcoming clinical trials
  • The Dermatologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with the research team to maintain high-quality trial execution
  • Serve as PI or Sub-I in assigned clinical trials
  • Conduct medical evaluations and assess participant eligibility
  • Monitor patient safety, adverse events, and treatment outcomes
  • Review and sign study-related documentation per protocol and regulations
  • Collaborate with study coordinators, nurses, and other research staff
  • Attend protocol training and ensure adherence to Good Clinical Practice (GCP)


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