Clinical Research Associate (CRA) - 174451

Responsibilities: of the CRA: · Lead site management support activities, including remote monitoring, site communication, and performance tracking to ensure enrollment, compliance, and milestone adherence. · Drive regulatory and document control processes by maintaining eTMF completeness, reviewing essential documents, and ensuring inspection readiness at all times. · Ensure data quality and integrity through proactive EDC review, query management, and identification/escalation of protocol deviations or risks. · Support full clinical trial lifecycle execution, including site start-up, activation, maintenance, and closeout in alignment with study timelines. · Collaborate cross-functionally with CRAs, CTMs, QA, and Data Management teams to resolve issues, mitigate risks, and maintain compliance with ICH-GCP and SOPs. Qualifications: of the CRA: · 2-5+ years of clinical research experience (CRO, sponsor, or site), in-house preferred · Prior experience in in-house CRA, CTA, or site management role preferred · Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes · Experience with eTMF, CTMS, and EDC systems · Solid understanding of document control, audit readiness, and ALCOA+ principles · Exposure to infectious disease, oncology, or cardiology trials · Bachelor's degree in Life Sciences, Nursing, Public Health, or related field Compensation: of the CRA: · Salary: $50,000 - $70,000 annually, commensurate with experience · Comprehensive Benefits: Medical, Dental, Vision (through Cigna), 401k, Sick leave required as by law, PTO (Paid Time Off), Paid Holidays This job opens for applications on 9/2/2026. Applications for this job will be accepted for at least 30 days from the posting date.