Principal Investigator (Endocrinologist)

Centricity Research•Morehead City, NC

9d•Onsite

About The Position

The Principal Investigator (PI) - Endocrinologist is responsible for the conduct and oversight of clinical research studies at the site level, with ultimate accountability for patient safety, regulatory compliance, and data integrity. This role is ideal for a physician who is passionate about advancing clinical research while maintaining a strong commitment to patient care. The PI serves as the physician of record for assigned studies and plays a hands-on role in both clinical care and research activities. In addition to research responsibilities, this position requires direct interaction with and care of both clinic and research patients. The PI works closely with research staff, clinical teams, sponsors, and investigators to ensure studies are conducted ethically, compliantly, and efficiently. Centricity Research values physicians who are not only clinically strong, but also collaborative, approachable, and team-oriented, creating a positive experience for patients and staff alike.

Requirements

Hold an MD or DO degree from an accredited medical school
Are board certified or board eligible in endocrinology
Have an active, unrestricted U.S. medical license and are in good standing
Are comfortable providing hands-on care to both clinic and research patients
Have experience in clinical research or a strong interest in serving as a Principal Investigator
Possess a solid understanding of FDA regulations, GCP, and clinical trial conduct (or are eager to learn)
Are collaborative, approachable, and value working as part of a multidisciplinary team
Communicate clearly and respectfully with patients, research staff, and sponsors
Take pride in delivering compassionate, patient-centered care
Are detail-oriented and committed to high-quality, compliant research

Nice To Haves

Prior experience as a Principal Investigator or Sub-Investigator
ACLS certification

Responsibilities

Serve as Principal Investigator for assigned clinical trials in accordance with FDA regulations and ICH-GCP
Provide direct medical care to both clinic patients and research participants, including protocol-required visits, assessments, and medical decision-making
Ensure the safety, rights, and welfare of all study participants
Maintain oversight of all trial-related medical decisions as outlined in FDA Form 1572
Supervise and support delegated research staff, ensuring appropriate training and compliance
Ensure studies are conducted in compliance with FDA regulations, GCP, IRB requirements, sponsor protocols, and company SOPs
Review and manage adverse events, serious adverse events, and unanticipated problems, ensuring timely and accurate reporting
Maintain familiarity with investigational products, including proper use and handling
Support patient enrollment and ensure informed consent is obtained appropriately and ethically
Maintain accurate, complete, and audit-ready study documentation and records
Disclose financial interests and comply with all regulatory and ethical requirements