Clinical Trials Sub-Investigator - Part-Time

AMR Clinical; Dearborn, Northern (MI, KY); Hybrid; USD 100,000 - 140,000; Part time

Job summary

AMR Clinical in Dearborn, MI is seeking a Sub Investigator to conduct clinical trials under the direction of the Principal Investigator. The role requires ensuring compliance with GCP, FDA regulations, and study protocols.

You will collaborate with study teams and sponsors, maintain regulatory documentation, monitor subject safety, and train clinical personnel. This is a part-time position with opportunities to impact multiple trials.

Qualifications

• Minimum 3 years of clinical research trial experience as PI or Sub-I.
• Active medical license (MD/DO) or PA/NP and license to practice in the state.
• Knowledge of FDA regulations, ICH guidelines and GCP.
• Ability to lead and manage study teams and maintain data integrity.
• Strong attention to detail and ability to work independently in a fast-paced environment.

Responsibilities

• Maintain a current license to practice medicine.
• Act as Sub Investigator for duration of trials and ensure protocol compliance.
• Conduct testing and rating scales per sponsor instructions and protocol.
• Complete documentation in paper and electronic form as required.
• Ensure data integrity and report SAEs as per protocol.
• Educate study team on patient populations and mechanism of action of study medication.
• Adhere to FDA1572 requirements and regulatory standards.
• Collaborate with site leadership to meet operational goals.

Education

MD/DO degree

Job description

AMR Clinical in Dearborn, MI is seeking a Sub Investigator to conduct clinical trials under the direction of the Principal Investigator. The role requires ensuring compliance with GCP, FDA regulations, and study protocols.

You will collaborate with study teams and sponsors, maintain regulatory documentation, monitor subject safety, and train clinical personnel. This is a part-time position with opportunities to impact multiple trials.