We are looking to add a full time onsite CRC to our growing team. This person will be working at a handful of sites in and or around the Downers Grove area. We are open to minimal coordinating experience and happy to train the right person!

Responsibilities include:

• Maintaining thorough knowledge of study-specific inclusion/exclusion criteria
• Direct patient care: vitals, phlebotomy
• Performing safety and efficacy assessments per protocol
• Vital signs, EKGs, and other assessments as assigned
• Responsible for timely data entry and query resolution
• Timely reporting of study events (SAEs, protocol deviations, etc.)
• Following subjects through study completion and creating a follow-up care plan with a physician, study subject, and primary care provider;
• Ensuring preparation for and facilitating of all study monitoring visits and following up promptly with monitor follow-up letters
• Prompt and professional communication with sponsors, representatives, and other study-related parties
• Maintaining professional and appropriate interactions with study subjects, caregivers, sponsors, and all other study-related personnel, and staff members
• Interacting with nursing/unit staff on a daily basis as applicable to ensure communication and accurate completion of source through daily chart review