Clinical Research Associate (CRA) - 174451

Zachary Piper Solutions; Bethesda (MD); Hybrid; USD 50,000 - 70,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401k

Paid time off

Paid holidays

Job summary

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 is a key liaison between investigative sites and study teams, driving site performance, regulatory compliance, and data quality.

This hybrid role is based in Bethesda, MD. Responsibilities include site monitoring, eTMF/CTMS/EDC oversight, regulatory documentation, data integrity, and collaboration with CRAs,

Qualifications

• 2-5+ years of clinical research experience (CRO, sponsor, or site).
• Strong knowledge of ICH-GCP, FDA regulations and trial processes.
• Experience with eTMF, CTMS and EDC systems.
• Exposure to infectious disease, oncology, or cardiology trials.

Responsibilities

• Lead site management support activities including remote monitoring and performance tracking.
• Drive regulatory and document control by maintaining eTMF completeness and inspection readiness.
• Ensure data quality through EDC review, query management, and deviation risk escalation.
• Support full trial lifecycle from site start-up to closeout in line with timelines.

Skills

Clinical research experience

ICH-GCP knowledge

eTMF/CTMS/EDC experience

Remote monitoring experience

Education

Bachelor's degree in Life Sciences or related field

Tools

eTMF

CTMS

EDC

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

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