Job Description

Piper Companies is seeking a Clinical Research Associate (CRA) to support the operational delivery of clinical trials across infectious disease, oncology, and cardiology programs. This role serves as a key liaison between investigative sites and study teams, driving site performance, regulatory compliance, and data quality. This role is hybrid out of Bethesda, MD. 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. Keywords: CRA, Clinical Research Associate, In-House, In house, TMF, Trial Master File, eTMF, Veeva, VeevaVault, CTA, Clinical Trial Associate, CTMS, Clinical Trial Management System, Cardiology, Oncology, Infectious Disease, Study Management, Study Timeline, Clinical Trial, Clinical Research, study start up, SSU, study closeout, EDC, electronic data capture, site activation, audit readiness, CRO, Clinical Research Organization, Pharmaceutical, Pharma, Biotech, SOP, Standard Operating Procedure, Query Management, Clinical Data, Regulatory, IRB, life sciences, regulatory documentations, eIRB, monitoring, centralized monitoring, data management, inspection readiness, protocol deviations, site maintenance, enrollment, hybrid #LI-BN1 #LI-HYBRID #J-18808-Ljbffr

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