Highlights:Salary: $75,000 - $90,000 based on ExpFull BenefitsMon - Fri Schedule; fully on on site Studies in allergy, asthma, vaccines, and more! Our Client:We are working with an exciting clinical trial site organization with over 25 locations, dedicated to advancing innovative therapies and improving lives by making clinical research more efficient and accessible. They focus on on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships help deliver high-quality data across a wide range of therapeutic areas!The Role:We are seeking an experienced CRC that values strong operations, thoughtful study execution, and team-based approach to clinical research! Coordinate all aspects of assigned clinical trials from site initiation through close-outConduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPsManage subject recruitment, informed consent, and retention activities (There is a recruitment team to support day to day recruitment)Ensure timely EDC data entry and resolution of queriesReport and follow up on AEs, SAEs, and protocol deviationsCollaborate with investigators, sponsors/CROs, labs, and internal teamsPrepare for and participate in monitoring visits, audits, and inspectionsMaintain regulatory documentation and ensure training compliance for amendments and systemsPerform study procedures such as phlebotomy, ECGs, and sample processing (as trained)Attend investigator meetings and provide cross-functional support as neededMaintain working knowledge of protocols, lab manuals, equipment calibration, and inventoryRequirements:3+ years exp as a CRC on sponsor backed trials Ability to work on site M-F (NO hybrid or remote days)