FULL-TIME
Posted Jun 16, 2026
50K–70K a year
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), 401(k), Sick leave required as by law, PTO (Paid Time Off), Paid Holidays.
This job opens for applications on 5/26/2026. Applications for this job will be accepted for at least 30 days from the posting date.
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), 401(k), Sick leave required as by law, PTO (Paid Time Off), Paid Holidays.
This job opens for applications on 5/26/2026. Applications for this job will be accepted for at least 30 days from the posting date.
Benefits
- Paid time off
- Dental insurance
- Health insurance
Additional Details
- City
- Bethesda
- State
- Maryland
- Country
- US
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