Principal Investigator Gastroenterologist
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Job Location:
Huntington Beach, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Huntington Beach California 92647 USA
In Person Contract Part Time
Minimum years of clinical research experience (required) 1
Description
We are seeking a Principal Investigator (Gastroenterologist) to join our team onsite in Huntington Beach California!
Overview
Our site partner is seeking a dedicated and research-oriented Physician Gastroenterologist to
join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator while continuing to provide high-quality medical care to adult patients within a clinical research setting.
This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.
Key Responsibilities
Serve as Principal Investigator or Sub-Investigator on multiple Phase IIV clinical trials.
Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
Provide medical oversight for clinical trial participants including safety assessments adverse event evaluations and ongoing care.
Collaborate closely with Clinical Research Coordinators Sponsors and Monitors to ensure protocol compliance and data integrity.
Review and sign off on source documents case report forms (CRFs) and regulatory documentation.
Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP FDA and sponsor requirements.
Participate in Site Initiation Visits (SIVs) Monitoring Visits and Audits as needed.
Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
Educate and counsel patients on study procedures informed consent and potential side effects.
Support recruitment efforts and promote patient retention in trials.
Qualifications
MD or DO degree from an accredited medical school.
Valid unrestricted medical license in the state of employment.
Board Certified or Board Eligible (BC/BE) in Gastroenterology
BC/BE in Family Medicine or Geriatric Medicine will also be considered.
Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.
Preferred Skills
Familiarity with FDA ICH-GCP and clinical trial protocols.
Experience managing or participating in industry-sponsored clinical trials.
Strong attention to detail and ability to document accurately.
Excellent interpersonal and communication skills for patient interaction and sponsor
collaboration.
Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
DEA license (preferred).
Open to Relocation - No
Job Roles and Responsibilities
Clinical Research
Gastroenterology
CTMS EMR and EDC Systems
Communication and Interpersonal Skills
Work Authorization
Required
Key Skills
- Epidemiology
- Public Health
- Bank Secrecy Act
- Bioinformatics
- Fraud
- Genetics
- Interviewing
- Law Enforcement
- Qualitative Research Interviewing
- Research Experience
- Next Generation Sequencing
- Writing Skills
