Physician Principal Investigator

Headlands Research

Escondido, CAFull-time and ContractorPosted Mar 22, 2026

130–160 an hour

Behavioral Health Market Context

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Job Description

ollaborative environment dedicated to diversity in clinical research.

Practice Info
• Two openings in the San Diego area: one at AMCR Institute in Escondido and one at Artemis Research near Serra Mesa
• AMCR Institute focuses on metabolic and immunologic research, including pre-diabetes, type 1 and type 2 diabetes, obesity, NAFLD/MASH, and vaccines
• Artemis Research specializes in psychiatry/neurology, internal medicine, and women's health studies

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

Compensation
• California Pay Range: $130-$160

Requirements
• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without
• Current and unencumbered license to practice as an MD or DO within the state of California 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
• IV experience preferred, but not required

Qualifications

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without
  • Current and unencumbered license to practice as an MD or DO within the state of California 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

Benefits

  • California Pay Range: $130-$160

Responsibilities

  • The successful candidates will contribute to advancing medical science within a supportive and collaborative environment dedicated to diversity in clinical research
  • 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


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