Clinical Research Associate
Piper Companies
115K–125K a year
Behavioral Health Market Context
Apply Nowvia Learn4Good
Benefits
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)
Job Description
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.
#J-18808-Ljbffr
. 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.
#J-18808-Ljbffr
Qualifications
- •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
Responsibilities
- •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
- •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
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