Part-time Psychiatrist - Clinical Research

Headlands Research • Riverside, CA

4d

About The Position

Headlands Research is seeking an experienced part-time psychiatrist to support the growth of the clinical research site at Artemis Institute for Clinical Research in Riverside, California. The role 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 at Headlands Research sites, ensuring that trials meet protocol requirements, regulatory standards, and ethical guidelines. The role also includes supporting and training site staff, overseeing participant safety and informed consent, and communicating with study stakeholders. Headlands Research describes diversity and inclusion as central to its mission and seeks to advance diversity in clinical trial research.

The California pay range is $130–$160 USD; the posting does not specify the pay period.

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 clinical research industry best practices.
• 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; the posting says candidates without this experience may also be considered.

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 and foster an inclusive, diverse, and professional research-team culture.
• 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.

What This Job Offers

• Job Type: Part-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree