Clinical Research Associate

Piper Companies; Indianapolis (IN); Remote; USD 90,000 - 120,000; Full time

Job summary

An innovative firm is seeking a Clinical Research Associate to join their dynamic team in a fully remote capacity. This role involves monitoring clinical trials and ensuring compliance with GCP and regulatory guidelines. The ideal candidate will have a strong background in oncology monitoring, proficiency in CTMS and EDC, and a passion for improving healthcare outcomes. With a competitive salary range and comprehensive benefits, this opportunity offers a chance to contribute to groundbreaking research while working from the comfort of your own home. If you are ready to make a difference in the clinical research field, this is the perfect role for you.

Benefits

Medical (Cigna)

Dental (Guardian)

Vision (VSP)

Sick leave

401K (Voya through ADP)

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 guidelines.
• Support subject recruitment and manage communication with sites.

Skills

Onsite oncology monitoring experience

CTMS

EDC

Microsoft Office Suite

Knowledge of GCP and ICH guidelines

Site management

Patient recruitment

Clinical trial documentation

Therapeutic knowledge in Phase 1 oncology trials

Education

Bachelor's degree in life sciences

Advanced degree in nursing or related field

Tools

CTMS

EDC

Microsoft Office Suite

Job description

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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.