Hybrid CRA: Lead Site Management & Data Quality

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

Benefits offered by this job

Medical, Dental, Vision insurance

401(k)

Sick leave

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 hybrid role is based in Bethesda, MD and acts as a liaison between investigative sites and study teams, driving site performance, regulatory compliance, and data quality.

Responsibilities include remote site monitoring, regulatory document control, data review in EDC, and collaboration with CRAs, CTMs, QA, and

Qualifications

• 2–5+ years of clinical research experience (CRO, sponsor, or site).
• Experience in-house CRA or site management preferred.
• Strong knowledge of ICH-GCP, FDA regulations, and trial processes.
• Experience with eTMF, CTMS, and EDC systems.
• Understanding of ALCOA+ document control and audit readiness.
• Experience in infectious disease, oncology, or cardiology trials.
• Bachelor’s degree in Life Sciences, Nursing, Public Health, or related field.

Responsibilities

• Lead site management and remote monitoring to support enrollment and compliance.
• Maintain regulatory and document control, ensure inspection readiness.
• Ensure data quality through EDC review and query management.
• Support full trial lifecycle: start-up, activation, maintenance, closeout.
• Collaborate with CRAs, CTMs, QA, and Data Management to resolve issues and mitigate risks.

Skills

Clinical research

ICH-GCP

Regulatory compliance

Cross-functional collaboration

Data quality focus

Education

Bachelor's degree in Life Sciences

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 hybrid role is based in Bethesda, MD and acts as a liaison between investigative sites and study teams, driving site performance, regulatory compliance, and data quality.

Responsibilities include remote site monitoring, regulatory document control, data review in EDC, and collaboration with CRAs, CTMs, QA, and