Part-time Psychiatrist - Clinical Research

Headlands Research•Riverside, CA
•$130 - $160•Onsite

About The Position

Headlands Research is seeking a part-time experienced psychiatrist to help grow its clinical research site at Artemis Institute for Clinical Research in Riverside, California. The position is ideally scheduled for up to three days per week, Monday through Thursday, from 8:00 a.m. to 2:00 p.m. The psychiatrist will lead and oversee clinical trials, support and mentor site staff, and help ensure trial conduct follows protocol requirements, regulatory standards, and ethical guidelines. The role also involves overseeing subject safety and informed consent, obtaining IRB approvals, and communicating with sponsors, monitors, regulators, and research network leadership.

Requirements

  • Eligible for or hold an active, unencumbered license to practice as an MD or DO in California.
  • Board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects in a fast-paced environment.

Nice To Haves

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials.

Responsibilities

  • Lead and oversee clinical trials at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay current on clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate with sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.
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