Part-time Psychiatrist - Clinical Research

Headlands Research • Maplewood, MN

2d • Onsite

About The Position

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.

Type: Regular Part-time Employee or 1099 Independent Contractor
Schedule: Site hours are Mondays through Fridays, 8:00am - 5:00pm; specific schedule is TBD.
Location: Onsite in Maplewood, MN (no capabilities for remote or hybrid work)
Reports to: Site Director

Requirements

• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.
• Nephrologist and Psychiatrist preferred, but open to considering a wide variety of specialties who can oversee outpatient-based pharma clinical research trials.
• Current and unencumbered license to practice as an MD or DO within the state of Minnesota required (or eligible for).
• Must be 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 simultaneously in a fast-paced environment.

Responsibilities

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

Benefits

• Competitive pay + annual performance incentives
• 401(k) plan with company match for full-time employees
• Company holidays
• A mission-driven culture focused on advancing medicine and improving patient outcomes

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level