Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote permanent position located based out of CST . The Clinical Research Associate (CRA) will travel to sites 8-10 days out of the month and be responsible for monitoring and clinical trials across the region for a leading Clinical Research Organization.
Responsibilities of the Clinical Research Associate include:
- Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines.
- Support subject recruitment and adapt recruitment plans as needed.
- Provide protocol training and manage communication with study sites.
- Assess site adherence to protocol and regulatory requirements, reporting quality issues.
- Track study progress, including regulatory approvals, enrollment, data collection, and query resolution.
- Maintain accurate site documentation, including visit reports and regulatory files.
Qualifications for the Clinical Research Associate include:
- At least 2 years of onsite oncology monitoring experience
- Proficiency in CTMS, EDC, and Microsoft Office Suite.
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience in site management, patient recruitment, and clinical trial documentation.
- Strong therapeutic and protocol knowledge in oncology trials.
- Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred).
Compensation for the Clinical Research Associate:
- Salary Range: $115,000-$125,000/year (USD)
- Comprehensive Benefits: Medical (Cigna), Dental (Guardian), Vision (VSP), sick leave if required by law, and 401K (Voya through ADP)
This job opens for applications on 1/16/26. Applications for this job will be accepted for at least 30 days from the posting date.
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