Clinical Research Associate

Piper Companies; Indiana (PA); Remote; USD 90,000 - 120,000; Full time

Job summary

Join a dynamic and innovative company as a Clinical Research Associate (CRA) in a remote role, where you will play a crucial part in monitoring clinical trials across the country. This position offers the opportunity to work with a leading Clinical Research Organization, ensuring compliance with regulatory guidelines and supporting patient recruitment. You will be involved in assessing site adherence to protocols and managing communication with study sites. This role is perfect for those passionate about oncology and clinical research, providing a comprehensive benefits package and competitive salary range. If you're ready to make a significant impact in the healthcare industry, this opportunity is for you.

Benefits

Medical Insurance (Cigna)

Dental Insurance (Guardian)

Vision Insurance (VSP)

401K (Voya through ADP)

Sick Leave if Required by Law

Qualifications

• 2+ years of oncology monitoring experience required.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.

Responsibilities

• Conduct site monitoring visits for compliance with GCP and ICH guidelines.
• Track study progress, including regulatory approvals and data collection.

Skills

Oncology Monitoring Experience

CTMS Proficiency

EDC Proficiency

Microsoft Office Suite

Knowledge of GCP

Knowledge of ICH Guidelines

Site Management Experience

Patient Recruitment Experience

Clinical Trial Documentation

Therapeutic Knowledge in Phase 1 Oncology Trials

Education

Bachelor's Degree in Life Sciences

Advanced Degree Preferred

Tools

CTMS

EDC

Microsoft Office Suite

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 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 :

• 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 Phase 1 oncology trials.
• Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred).

Compensation for the Clinical Research Associate :

• Salary Range : $90,000-$120,000 (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 4 / 21. Applications for this job will be accepted for at least 30 days from the posting date.