Clinical Trials Sub-Investigator: Lead Studies & Care

Alliance for Multispecialty Research LLC; Dearborn (MI); On-site; USD 60,000 - 110,000; Part time

Job summary

AMR Clinical in Dearborn, MI is seeking a Sub Investigator to conduct clinical trials per protocol and GCP under the Principal Investigator. You will collaborate with the study team, regulatory personnel, and sponsors to safeguard subject welfare and data integrity.

The role requires a current medical license, 3+ years of clinical research experience as PI or Sub-I, and knowledge of FDA/ICH/GCP guidelines. The position involves documentation, evaluations, and collaboration with site leadership.

Qualifications

• At least 3 years experience conducting clinical research trials as either PI or Sub-I.
• Active license to practice medicine within the state.
• Understanding of FDA regulations, ICH guidelines, and Good Clinical Practices.

Responsibilities

• Maintain a current license to practice medicine.
• Assume responsibility as the Sub Investigator for the duration of the clinical trials.
• Conduct testing and rating scales per sponsors instructions and protocols.
• Completion of documentation, paper and electronic as required per protocol.
• Provide detailed study related documentation as required and ensure data integrity.
• Perform evaluations on subjects as needed per the protocol.
• Perform physicals per study protocol, as needed.
• Evaluate subjects for clinical research trials based on their past medical history.

Skills

Clinical research

Leadership

Regulatory knowledge

Documentation

Attention to detail

Education

MD/DO/PA/NP license

Job description

AMR Clinical in Dearborn, MI is seeking a Sub Investigator to conduct clinical trials per protocol and GCP under the Principal Investigator. You will collaborate with the study team, regulatory personnel, and sponsors to safeguard subject welfare and data integrity.

The role requires a current medical license, 3+ years of clinical research experience as PI or Sub-I, and knowledge of FDA/ICH/GCP guidelines. The position involves documentation, evaluations, and collaboration with site leadership.