Dermatologist - Clinical Research Investigator

ECN Clinical; Chandler (AZ); On-site; USD 74,000 - 185,000; Part time

Job summary

ECN Clinical is seeking a Dermatologist - Clinical Research Investigator to join our clinical team on a part-time per diem basis. You will serve as Principal Investigator or Sub-Investigator on multiple trials, overseeing examinations, safety assessments, and regulatory compliance.

The ideal candidate holds an MD/DO, a medical license in the employment state, and Dermatology board status (BC/BE), with GCP certification or willingness to obtain it prior to start.

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 Dermatology.
• GCP certification or willingness to obtain prior to start.
• Minimum of 1 year of clinical practice; clinical research experience preferred.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV trials.
• Perform physical exams and assessments for protocol screening and enrollment.
• Evaluate patient eligibility per protocol criteria.
• Oversee safety assessments, adverse events, and ongoing care.
• Collaborate with coordinators, sponsors, and monitors for protocol compliance.
• Review and sign source documents and regulatory paperwork.
• Maintain trial documentation per ICH-GCP/FDA requirements.
• Participate in Site Initiation Visits, Monitoring Visits, and Audits as needed.
• Educate patients on procedures, consent, and potential side effects.
• Support recruitment and patient retention in trials.

Skills

Clinical oversight

Patient care

Regulatory documentation

Communication skills

Education

MD or DO

Board Certified/Eligible in Dermatology

Medical license in state of employment

GCP certification

Board Certification in Family Medicine or Geriatric Medicine (considered)

1 year clinical practice experience

Job description

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Dermatologist - Clinical Research Investigator

ECN Clinical is seeking a dedicated and research-oriented Dermatologist - Clinical Research Investigator 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 Dermatology.
• 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).