Clinical Research Associate

Piper Companies; United States; Remote; USD 115,000 - 125,000; Full time

Benefits offered by this job

Medical (Cigna)

Dental (Guardian)

Vision (VSP)

401K (Voya through ADP)

Job summary

A leading clinical research organization is seeking a Clinical Research Associate (CRA) for a remote permanent position based out of CST. The CRA will conduct site monitoring visits, support subject recruitment, and manage communication with study sites. Candidates should have at least 2 years of oncology monitoring experience and a bachelor's degree in life sciences or nursing. The role offers a competitive salary range of $115,000-$125,000/year along with comprehensive benefits including medical, dental, vision, and a 401K plan.

Qualifications

• At least 2 years of onsite oncology monitoring experience.
• Strong therapeutic and protocol knowledge in oncology trials.

Responsibilities

• 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.
• Track study progress, including regulatory approvals, enrollment, data collection, and query resolution.
• Maintain accurate site documentation, including visit reports.

Skills

Oncology monitoring experience

Proficiency in CTMS

Proficiency in EDC

Proficiency in Microsoft Office Suite

Knowledge of GCP

Knowledge of ICH guidelines

Experience in site management

Patient recruitment

Clinical trial documentation

Education

Bachelor's degree in life sciences, nursing, or related field

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.