What are the responsibilities and job description for the Clinical Research Coordinator position at Emerge Research Institute?
Company Description
Emerge Research Institute is an embedded clinical research site management organization (SMO) operating across Metro Detroit. We deploy directly within established physician practices — supplying staff, equipment, and trial infrastructure — so studies reach patients where they already receive care. Our current therapeutic focus includes pulmonology, ENT, pain/spine, and internal medicine.
Role Description
Full-time, on-site CRC role embedded within a physician practice in the Metro Detroit area. You will manage day-to-day trial operations across one or more active studies: coordinating subject visits, maintaining regulatory binders, executing informed consent, entering data into sponsor EDC systems, and serving as the primary site contact for CRAs and sponsors. This is an execution-heavy role — you own the study operations.
Qualifications
- 2 years CRC experience, with at least 1 year in pulmonology, allergy/immunology, or ENT preferred (or 4 years general CRC)
- Hands-on experience with at least one major EDC platform (Medidata Rave, Oracle InForm, Veeva Vault)
- Working knowledge of ICH-GCP, 21 CFR Parts 11/50/54/56/312
- ACRP-CP or CCRC certification preferred
- Experience coordinating sponsor monitoring visits and responding to queries
- Strong independent execution — this role operates with limited daily oversight
- Bachelor's degree in life sciences, nursing, or health sciences