Jobless Developer
Centricity Research logo

Posted 5 months ago

Open

Principal Investigator (Endocrinologist)

Morehead CityRemote

AI Summary

Serves as Principal Investigator for clinical trials in endocrinology, overseeing study conduct, patient safety, regulatory compliance, and data integrity while providing direct medical care to both clinic and research participants.

About this role

About the Role

The Principal Investigator (PI) - Endocrinologistis responsible forthe 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 whilemaintaininga 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, creatinga positiveexperience for patients and staff alike.

WhatYou’llDo

  • Serve as Principal Investigator for assigned clinical trialsin accordance withFDA 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, ensuringappropriate trainingand 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, ensuringtimelyandaccuratereporting
  • Maintain familiarity with investigational products, including proper use and handling
  • Support patient enrollment and ensure informed consent is obtained appropriately and ethically
  • Maintainaccurate, complete, and audit-ready study documentation and records
  • Disclosefinancial interestsandcomply withall 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
  • Arecomfortable providing hands-on care to bothclinicand 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 notrequired:

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

Why Centricity Research?

Our Mission

We connect people to scientific advancements through groundbreaking research within adeeplyhuman experience.

Our Core Values

  • Quality:We aim for excellence and integrity in everything we do-because lives depend on it.
  • Care:We show up for each other, our customers, and our mission-always going the extra mile.
  • Be the Change You Seek:We'readaptable, forward-thinking, and constantly improving-for the betterment of all.
  • One Team:We collaborate, support one another, and succeed together.
  • Grow for Good:We grow with purpose-to expand access to research andimproveglobal health.
  • Own It:We take initiative, deliver results, and follow through-with passion and accountability.

Skills

ACLsAdverse Event ReportingClinical Trial ConductFDA Form 1572FDA RegulationsICH-GCPInformed ConsentInvestigational ProductsIRB RequirementsStudy Documentation

Explore related jobs

Browse these categories

Market data for this role

All reports →