What are the responsibilities and job description for the Clinical Research Associate position at Piper Companies?
Piper Companies is seeking a Clinical Research Associate (CRA) to join a global leader in clinical research and healthcare analysis for a remote position. The Clinical Research Associate (CRA) will monitor and participate in clinical trials across the country for a leading Clinical Research Organization.
Responsibilities of the Clinical Research Associate include:
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.
- 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 Phase 1 oncology trials.
- Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred).
- Salary Range: $90,000-$120,000
- Comprehensive Benefits: Medical (Cigna), Dental (Guardian), Vision (VSP), sick leave if required by law, and 401K (Voya through ADP)
Salary : $90,000 - $120,000
