Clinical Research Associate

Piper Companies; Golden Horseshoe; Remote; USD 90,000 - 120,000; Full time

Job summary

An established industry player in clinical research is seeking a Clinical Research Associate to join their remote team. This role involves monitoring clinical trials, ensuring compliance with regulatory guidelines, and supporting subject recruitment. The ideal candidate will have a strong background in oncology monitoring and be proficient in relevant tools such as CTMS and EDC. This is a fantastic opportunity to contribute to impactful research while enjoying a comprehensive benefits package and a supportive work environment. If you are passionate about advancing healthcare through clinical trials, this position is perfect for you.

Benefits

Medical Insurance (Cigna)

Dental Insurance (Guardian)

Vision Insurance (VSP)

401K (Voya through ADP)

Sick Leave

Qualifications

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

Responsibilities

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

Skills

Oncology Monitoring

CTMS

EDC

Microsoft Office Suite

GCP Knowledge

ICH Guidelines

Site Management

Patient Recruitment

Clinical Trial Documentation

Education

Bachelor's degree in life sciences

Advanced degree (preferred)

Tools

CTMS

EDC

Microsoft Office Suite

Job description

Join to apply for the Clinical Research Associate role 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:

• 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 will be accepted for at least 30 days from the posting date.

Additional Details:

• Seniority level: Entry level
• Employment type: Full-time
• Job function: Research, Analyst, and Information Technology
• Industries: Business Consulting and Services

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