Laboratory Research Associate

The Clinical Laboratory Research Associate (CRA) will join our dedicated clinical laboratory team and be responsible for the analysis and data collection for clinical laboratory device trials. They will serve as a point of contact for multiple clinical trials and specimen procurements, while preparing and maintaining regulatory records, protocols, supply accountability, case report forms (CRFs), shipping records, de-identification and ID crosswalk. They will participate in site sponsor visits, trainings, and inspections. They will assist in assessing the feasibility of clinical study protocols, development of workflow procedures, and drafting of Institutional Review Board (IRB) submissions. They will maintain the quality and integrity of the clinical data through completion of eCRF database and on-site source verification records while working with sponsors to resolve queries and helps ensure all study deliverables are completed per study timelines. The CRA will manage all trial data files for studies and help train new/ ad hoc research staff on protocol requirements, source documentation, EDC system, case report form completion, and workflow.

Minimum Required

Associate’s degree WITH at least 2 years of clinical laboratory or research experience

Preferred

Bachelor’s degree in scientific discipline or health care