Psychiatrist - Clinical Research Investigator

ECN Operating LLC; Chandler (AZ); On-site; USD 120,000 - 180,000; Part time

Job summary

Elite Clinical Network (ECN) in Chandler, AZ is seeking a Physician – Psychiatrist to serve as Principal Investigator or Sub-Investigator for Phase I–IV trials.

This part-time/per-diem role combines providing medical oversight, conducting exams, ensuring protocol adherence, and collaborating with study coordinators, sponsors, and monitors.

A valid medical license, board certification/eligibility in Psychiatry, and GCP training are required.

Qualifications

• MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment.
• Board Certified or Board Eligible in Psychiatry.
• BC/BE in Family Medicine or Geriatric Medicine considered.
• GCP certification or willingness to obtain prior to start.
• Minimum of 1 year of clinical practice; prior clinical research preferred.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV trials.
• Perform comprehensive physical exams and assessments for screening and enrollment.
• Evaluate patient eligibility based on protocol criteria.
• Provide medical oversight for trial participants, including safety assessments.
• Collaborate with CRAs, sponsors, and monitors to ensure protocol compliance.
• Review source documents and regulatory documentation.
• Maintain trial documentation in compliance with ICH-GCP and FDA requirements.
• Participate in Site Initiation Visits, Monitoring Visits, and Audits as needed.
• Manage chronic and acute conditions per protocol guidelines.
• Educate and counsel patients on study procedures and side effects.
• Support recruitment efforts and patient retention in trials.

Skills

Strong communication

Attention to detail

Team collaboration

EMR proficiency

Clinical judgment

Education

MD or DO degree

Medical license in the state

GCP certification

Tools

CTMS

EMR systems

Job description

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Psychiatrist 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 I–IV 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 Psychiatry.
• 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).