Principal Investigator (Endocrinologist)

Join Us at Centricity Research! 

Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.

About the Role 

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. 

What You’ll Do 

• 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 

You Might Be a Great Fit If You: 

• 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 

Preferred but not