About the job
At Headlands Research, we are committed to revolutionizing clinical trial delivery across our communities. As a premier network of advanced clinical trial sites, we utilize state-of-the-art technology alongside exceptional support services to enhance outreach and participation in clinical research. Established in 2018, our rapidly expanding organization operates over 20 sites across the United States and Canada, with ambitious plans for continued growth.
Advancing Diversity in Clinical Trials
Diversity is not merely a checkbox for us; it is integral to our mission. We are dedicated to advancing medical science by fostering diversity in all aspects of clinical trial research. From our team composition to participant demographics, inclusivity is at the core of our operations.
Your Role Awaits
Are you ready to make a significant impact? We are looking for an experienced physician to serve as a principal or sub-investigator to support the growth of our clinical research site in Detroit, Michigan, on a PRN or Per-Diem basis (also open to 1099 independent contractors).
Why Become Part of Our Team?
- Flexible Schedule: Work on your own terms, with a schedule that accommodates your lifestyle.
- Dynamic Team Environment: Contribute to the development of a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With robust support and a collaborative culture, you will flourish in an environment where your contributions truly matter. A high degree of professionalism distinguishes Headlands.
Key Responsibilities:
- Lead and manage clinical trials at Headlands Research sites, ensuring adherence to protocol requirements, regulatory standards, and ethical guidelines.
- Provide leadership and mentorship to site staff, promoting a culture of inclusivity, diversity, and professionalism within the research team.
- Engage in investigator meetings and educational initiatives to remain informed about advancements in clinical research and diversity efforts.
- Secure IRB approval for study initiation and any protocol amendments.
- Oversee subject safety, compliance with trial conduct, and the informed consent process.
- Effectively communicate with stakeholders, including sponsors, monitors, regulators, and research network leadership.
- Facilitate ongoing training and development for staff to ensure optimal trial operations.
