Senior Clinical Research Associate

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

📋 Description

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

• Evaluate and identify potential research sites for participation.

• Organize initial study activities, including necessary regulatory documentation and the contract and budget processes.

• Conduct Pre-Study Site Visits (PSSVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs).

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

• Monitor site performance and provide continuous support throughout the study lifecycle.

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

• Collaborate with sites and study teams to enhance data quality, ensure participant safety, and promote study success.

• Assist in site closure and the fulfillment of study obligations.

• Travel to investigative sites to work alongside sites, sponsors, and global study teams.

⛳️ Requirements

• Bachelor’s Degree or a Nursing Degree.

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

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

• Must be willing to travel 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 live within the Midwest territory.

• Ability to travel to investigative sites around 8–10 days each month.

🏝️ Benefits

• Competitive benefits package tailored to location.

• A workplace that promotes inclusivity and equity.

• Equal employment opportunities for all candidates.

• Clear compensation structure and emphasis on pay equity.