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

📋 Description

• Oversee clinical research operations at investigative sites involved in global clinical trials.

• Evaluate and select potential research locations.

• Organize study initiation tasks, including regulatory documentation and the management of contracts and budgets.

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

• Educate site staff on protocol specifications, data gathering, and safety reporting procedures.

• Supervise site performance and offer continuous support during the study's lifecycle.

• Ensure informed consent procedures, safety reporting, and adherence to regulatory standards.

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

• Assist with site closure procedures and fulfill all study-related requirements.

⛳️ Requirements

• Bachelor’s Degree or a Nursing Degree.

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

• At least 2 years of essential experience in monitoring Oncology clinical trials.

• Must be located within the Midwest region of the United States.

• Travel within the designated area is necessary; 8–10 days per month.

• Prior experience in full-service monitoring is preferred.

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

🏝️ Benefits

• Competitive benefits package tailored to location.

• An inclusive and equitable work environment.

• Equal employment opportunity for all candidates.