Job Details
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