Physician - Clinical Trials - MD/DO

Headlands Research; Charlotte (NC); On-site; USD 150,000 - 230,000; Full time

Job summary

Headlands Research in Charlotte, NC is seeking an experienced Principal Investigator or Sub-Investigator to help launch a new clinical research site. You will lead and oversee trials, ensure protocol and regulatory compliance, and mentor site staff.

If you are an MD/DO, board-certified or eligible, with prior investigator experience and strong leadership, we want to talk. We offer flexible schedules, part-time or full-time options, and a collaborative, diverse team.

Qualifications

• Requires MD/DO license to practice in North Carolina.
• Board-certified or board-eligible for clinical research.
• Proven experience as Principal Investigator or Sub-Investigator.

Responsibilities

• Lead and oversee clinical trials at Headlands Research sites, ensuring protocol compliance and ethics.
• Mentor and guide site staff fostering inclusivity and professionalism.
• Participate in investigator meetings and educational initiatives to stay current in research.
• Obtain IRB approval for study initiation and protocol modifications.
• Oversee subject safety, trial conduct, and informed consent processes.
• Communicate with sponsors, monitors, regulators, and leadership about study progress.
• Provide ongoing training and support to research staff.

Skills

Leadership

Communication

GCP knowledge

Education

MD/DO

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 new 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 Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Charlotte area. Whether you're a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We're flexible—we're open to part-time or full-time commitments with flexible schedules.

Why Join Us?

• Flexible Schedule: Work on your terms, with a schedule that fits your life.
• Unlimited Potential: The sky's the limit. We're open to up to 40 hours per week, allowing you to maximize your impact.
• Dynamic Team Environment: You'll help Headlands Research 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 required.
• Active and unencumbered license to practice as an MD or DO within the state of North Carolina 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.

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.