Physician Clinical Trials MDDO

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 were 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 weve 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 isnt just a checkbox for usits central to our mission. Were 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 Were seeking an experienced Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Memphis area. Whether youre 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. Were flexiblewere 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 skys the limit. Were open to up to 40 hours per week allowing you to maximize your impact.
• Dynamic Team Environment: Youll 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 youll 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 Tennessee 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.