This is a fully remote position, open to applicants in Michigan.

📋 Description

• Oversee clinical research operations at investigative sites involved in Worldwide clinical trials

• Identify and evaluate potential research sites

• Coordinate the initiation of studies, including handling regulatory documentation, contracts, and budget processes

• Perform Pre-Site Selection, Study Initiation, Interim Monitoring, and Closeout Visits

• Educate site personnel on protocol requirements, data collection methods, and safety reporting procedures

• Monitor site performance and provide continuous support for study maintenance

• Ensure adherence to informed consent, safety reporting, and regulatory compliance

• Collaborate with sites and study teams to enhance data quality, ensure participant safety, and achieve study objectives

• Assist with site closeout activities and fulfill study requirements

• Travel to investigative sites approximately 8–10 days per month

⛳️ Requirements

• Bachelor's Degree or a Nursing Degree

• Over 5 years of experience as a regional, traveling Clinical Research Associate

• Travel required within the designated region; approximately 8–10 days per month

• Preferred experience in full-service monitoring

• Strong understanding of clinical trial processes, site management, and regulatory requirements

• Candidates must be residents within the East Coast territory

• Capability to travel to investigative sites around 8–10 days per month

🏝️ Benefits

• Competitive benefits package based on location

• Inclusive and equitable workplace

• Equal employment opportunities