Principal Investigator

Headlands Research, Inc.; San Diego (CA); On-site; USD 138,000 - 207,000; Full time

Benefits offered by this job

Flexible schedule

Diverse team environment

Job summary

Headlands Research, Inc. in San Diego seeks an experienced physician to lead and grow a clinical research site within our Artemis Institute network.

You will oversee trials, ensure protocol compliance, and mentor staff across a diverse team of coordinators and investigators. The role requires an active CA MD/DO license, board eligibility or certification, and a proven track record in regulatory adherence and trial leadership.

Qualifications

• Experience as Principal Investigator or Sub-Investigator is highly desirable.
• Active California MD/DO license required or eligible.
• Board certification or eligibility is preferred.
• Strong communication and leadership capabilities.
• Solid understanding of regulatory and GCP standards.
• Ability to manage multiple trials and sites efficiently.

Responsibilities

• Lead and oversee clinical trials at Headlands Research sites with protocol compliance.
• Mentor site staff to promote inclusivity, diversity, and professionalism.
• Participate in investigator meetings and ongoing education on trial advancements.
• Obtain IRB approval for study initiation and protocol amendments.
• Oversee subject safety, trial conduct, and informed consent processes.
• Communicate with sponsors, monitors, regulators, and leadership.
• Provide ongoing training and support to research staff.

Skills

PI/Sub-I experience

CA MD/DO license

Board-certified/eligible

Leadership skills

Regulatory knowledge

Multi-project management

Education

MD/DO license in CA

Board certification

Job description

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.

Join Us in Improving Lives through Clinical Research

At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.

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.

Why Join Us?

• Flexible Schedule: Work on your terms, with a schedule that fits your life. This could be part-time or full-time work.
• Dynamic Team Environment: You'll help Headlands 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 Headlands.

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.

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.

$100 - $150 USD

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Need Assistance?

Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact [e-mail] for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.