Clinical Research Associate (CRA)

Piper Companies is seeking an experienced Clinical Research Associate (CRA) to join our client’s team. This opportunity is with an industry-leading Clinical Research organization supporting one of the top pharmaceutical companies in the world. The CRA will play a critical role in monitoring and managing clinical trials, ensuring compliance with regulatory requirements, and maintaining high standards of data integrity and patient safety.

Locations for the Clinical Research Associate: Illinois, Indiana, Missouri, Michigan, Ohio, California, Tennessee, Oklahoma, Pennsylvania, Washington, Oregon

Responsibilities for the Clinical Research Associate:

• Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Conduct site visits, including pre-study, initiation, monitoring, and close-out visits.
• Review and verify case report forms (CRFs) and source documents for accuracy and completeness.
• Ensure timely and accurate reporting of adverse events and protocol deviations.
• Provide training and support to site staff on study protocols, procedures, and regulatory requirements.
• Maintain effective communication with study sites, investigators, and other stakeholders.
• Assist in the preparation and review of study-related documentation, including informed consent forms, study manuals, and monitoring plans.
• Participate in study team meetings and provide updates on site status and study progress.

Qualifications for the Clinical Research Associate:

• At least 2 years of experience as an On-site CRA.
• Comfortable with up to 70% travel (2-3 days per week).
• Must have a valid driver’s license.
• Must be comfortable handling questions regarding RECIST (Response Evaluation Criteria in Solid Tumors) and CTCAE (Common Terminology Criteria for Adverse Events).
• Strong understanding of clinical trial processes and regulatory requirements.
• Excellent organizational and time management skills.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Bachelor’s degree in a related field (e.g., life sciences, nursing, pharmacy).

Compensation/Benefits for the Clinical Research Associate:

• Salary: $100,000 - $120,000
• Benefits: Work-life balance with discretionary leave, 10 paid holidays, regional travel, exposure to challenging and interesting trials in oncology.