Offer summary

Qualifications:

Eligible for or active unencumbered license to practice as an MD or DO in California., Must be board-certified or board-eligible., Excellent communication and leadership skills., Familiarity with regulatory requirements and Good Clinical Practice (GCP) guidelines..

Key responsabilities:

Lead and oversee clinical trials ensuring compliance with protocol and regulatory standards.

Provide leadership and mentorship to site staff, promoting inclusivity and professionalism.

Obtain IRB approval for study initiation and modifications.

Communicate effectively with stakeholders including sponsors and research network leadership.

Job description

Overview:

The Company

Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women’s Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials. Together with 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.

This Primary Investigator role will be based at our San Diego, CA location and is a part time .

Travel: 5%

Work Schedule: Monday & Thursday - 8:30am-5pm / Tuesday, Wednesday, and Friday 7:00am-3:30 pm (You will work 3 days a week with the option of working 4 days every other week.)

The Role

Join Us in Improving Lives through Clinical Research

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us—it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? We're seeking an experienced physician to help us grow our clinical research site at Artemis Institute for Clinical Research in San Diego, CA, primarily physicians with previous experience serving as a Principal Investigator (PI) on vaccine clinical trials or other metabolic and medical clinical trials

Why Join Us?

Flexible Schedule: Work on your terms, with a schedule that fits your life.

Dynamic Team Environment: You'll help Artemis Institute for Clinical Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Artemis.

Responsibilities:

Lead and oversee clinical trials conducted at Artemis Institute for Clinical Research, 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.

Qualifications:

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.
Active DEA license
IV experience strongly preferred

Required profile