Clinical Research Physician

Headlands Research is seeking an experienced physician to join their team at Headlands Research - El Paso in a contract or PRN/Per-Diem capacity.

In this role, the clinician will serve as a Principal Investigator or Sub-Investigator to help grow the clinical research site while championing diversity in clinical trials. The ideal candidate will provide clinical leadership, oversee trial conduct and subject safety, and collaborate with a dynamic multidisciplinary team.

Practice Info

• Leading network of advanced clinical trial sites
• Headlands Research - El Paso site location
• Clinical research setting
• Collaborate with clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists

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.

Shift & Schedule

• Contract or PRN/Per-Diem
• Flexible schedule

Qualifications

• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials preferred, though candidates without experience will be considered.
• Eligible for or active unencumbered license to practice as an MD or DO within the state of Texas 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.