Clinical Research Associate II – Metabolic

This is a fully remote position, open to applicants in Arizona, +1 more state.

📋 Description

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

• Evaluate and identify potential research locations

• Organize study initiation tasks, encompassing regulatory documentation as well as contract and budget procedures

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

• Educate site staff on protocol stipulations, data collection methods, and safety reporting

• Supervise site performance and offer continuous support throughout the study duration

• Guarantee informed consent, safety documentation, and adherence to regulatory standards

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

• Assist with site closure and fulfill study obligations

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

⛳️ Requirements

• Bachelor’s Degree or a Nursing Degree

• Minimum of 3 years as a regional, traveling Clinical Research Associate

• Background in monitoring Cardiometabolic and Hypertension clinical trials

• Must travel within the designated region; 8–10 days of travel per month

• Experience in comprehensive monitoring is preferred

• In-depth understanding of clinical trial processes, site management, and regulatory guidelines

• Candidates are required to reside within the specified territory

• Capacity to support site visits and study operations across the Central / West Coast of the United States

🏝️ Benefits

• Competitive benefits package based on location

• Inclusive and equitable work environment

• Equal employment opportunities for all

• Transparent compensation and commitment to pay equity