Physician - Clinical Trials - MD​/DO Las Cruces, NM

About Headlands Research

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.

We are not just building a clinical trial network; we are working to bring trials to underserved communities and new treatments to market. We are a family of next‑generation sites where technology meets unparalleled support and participant engagement reaches new heights.

Diversity is central to our mission. We promote inclusivity in every facet of clinical research—from team composition to participant demographics.

We are seeking an experienced Principal Investigator or Sub‑Investigator to help us grow a new clinical research site in the Las Cruces area. Whether you are a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or another area of medicine, your passion for improving patient outcomes is what matters most. If you have prior Investigator experience, we want to talk with you.

We are flexible and open to part‑time or full‑time commitments with flexible schedules.

• Flexible Schedule
  :
  Work on your terms, with a schedule that fits your life.
• Unlimited Potential
  :
  Up to 40 hours per week to maximize impact.
• Dynamic Team Environment
  :
  Build a diverse, talented team of coordinators, assistants, physicians, providers, and recruitment specialists.

• Lead and oversee clinical trials at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
• Provide leadership and mentorship to site staff, fostering inclusivity, diversity, and professionalism.
• Participate in investigator meetings and educational initiatives to stay updated on research advancements.
• Obtain IRB approval for study initiation and protocol modifications.
• Oversee subject safety, trial conduct compliance, and informed consent processes.
• Communicate effectively with sponsors, monitors, regulators, and research network leadership.
• Provide ongoing training and support to research staff.

• Previous experience as a Principal Investigator or Sub‑Investigator for clinical research trials.
• Active, unencumbered MD or DO license in New Mexico.
• Board‑certified or board‑eligible.
• Excellent communication and leadership skills.
• Familiarity with GCP guidelines and regulatory requirements.
• Strong organizational skills and attention to detail.

As set forth in Headlands Research’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.