Principal Investigator MD/DO

Headlands Research•San Diego, CA

13d•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. We are seeking an experienced physician to help us grow our clinical research site at Artemis Institute for Clinical Research in San Diego, CA. We are not just building a clinical trial network; we are working to bring clinical trials to underserved communities and treatments to market. We champion diversity in clinical trials, as it is central to our mission to advance medical science by promoting diversity in every facet of clinical trial research.

Requirements

Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.
Eligible for or active unencumbered license to practice as an MD or DO within the state of California required
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 conducted at Headlands Research sites, 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.