Nephrologist (Clinical Trails) - Part-time - Anchorage, AK

ProTouch Staffing

Anchorage, AKPart-time and Contractor

Behavioral Health Market Context

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Job Description

llaborate with the research team to maintain high-quality trial execution.

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).

Qualifications:
• MD or DO with an active CA medical license.
• Board-certified in Nephrology.
• Interest in clinical research (prior experience preferred; training provided if needed).
• Strong communication, teamwork, and organizational skills.

Benefits:
• Flexible schedule: 0-8 hours/week.
• Professional growth opportunities in clinical research.
• Contribute to advancing dermatology treatments and patient outcomes.

For more information, please reach out to Dheeraj Mohan: at (469) 430-0547 or by Email: at [email protected].

Qualifications

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

Benefits

  • Flexible schedule: 0-8 hours/week
  • Professional growth opportunities in clinical research
  • Contribute to advancing dermatology treatments and patient outcomes

Responsibilities

  • 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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