Sub-Investigator

Associate Clinical Investigator (PRN)

Location: US Based - Remote
Engagement Type: PRN / Contract (approximately 5–10 hours per week)
Onsite Requirement: Yes

Overview

The Clinical Research Sub-Investigator (SI) supports the Principal Investigator in the conduct of clinical research trials at various US based sites. The SI performs delegated clinical and research duties, ensuring compliance with study protocols, ethical standards, and regulatory guidelines, under the direct supervision of the PI.

Key Responsibilities

• Conduct clinical assessments and patient study visits.
• Assist the PI in participant screening, eligibility determination, and informed consent discussions.
• Document patient data, adverse events, and concomitant medications in study records.
• Perform assessments as required by the protocol.
• Collaborate closely with the PI, study coordinators, and sponsor monitors.
• Review study documentation for accuracy and completeness.
• Ensure adherence to FDA, ICH-GCP, and institutional policies.

Qualifications

• US Licensed MD, DO, NP, or PA
• Experience in Neurology, Pulmonology, Dermatology, or Internal Medicine (Cardiology, Infectious Disease, Endocrinology, Gastroenterology, and Rheumatology focus) required/preferred.
• Prior experience as a Sub-Investigator or Clinical Research Physician strongly desired.
• Good Clinical Practice (GCP) and Human Subjects Protection certification required.
• Excellent attention to detail, clinical documentation, and patient interaction skills.

Schedule & Compensation

• PRN (as-needed) engagement — 5–10 hours per week on average.
• FMV-based hourly or per-study compensation commensurate with experience.