Clinical Research Physician
5 days ago
Transforming Lives through Clinical Research
At Headlands Research, we're dedicated to advancing medical science by promoting diversity in every facet of clinical trial research. As a Principal Investigator or Sub-Investigator, you'll play a pivotal role in leading and overseeing clinical trials conducted at our sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
Key Responsibilities:
- Lead and oversee clinical trials, ensuring compliance with protocol requirements and regulatory standards.
- Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism.
- 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 New Mexico 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.
Why Headlands Research?
We're an equal-opportunity employer and welcome applicants from all backgrounds and experiences. Join us in our mission to advance medical science and promote diversity in clinical trial research.
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