Oncology Clinical Research Associate (CRA)

Piper Companies; British Columbia; On-site; USD 100,000 - 140,000; Full time

Job summary

An established industry player is looking for a dedicated Clinical Research Associate to join their dynamic team. In this pivotal role, you will monitor clinical trials, ensuring compliance with regulatory standards while maintaining data integrity and patient safety. This position offers an exciting opportunity to work with a leading Oncology Clinical Research organization, where you will collaborate with top pharmaceutical companies. If you are passionate about clinical research and thrive in a fast-paced environment, this role is perfect for you. Join a team that values excellence and innovation in the healthcare sector.

Benefits

Comprehensive Medical Benefits

Dental Insurance

Vision Insurance

401K

Paid Time Off

Sick Leave

Holidays

Qualifications

• 2+ years of experience as an On-site CRA.
• Strong understanding of clinical trial processes and regulatory requirements.

Responsibilities

• Monitor clinical trials for compliance with protocols and regulations.
• Conduct site visits and provide training to site staff.
• Ensure accurate reporting of adverse events and protocol deviations.

Skills

Clinical Trial Monitoring

Regulatory Compliance

Good Clinical Practice (GCP)

Communication Skills

Organizational Skills

Interpersonal Skills

Time Management

Education

Bachelor’s degree in life sciences

Job description

Piper Companies is seeking an experienced Clinical Research Associate (CRA) to join our client’s team. This opportunity is with an industry-leading Oncology Clinical Research organization supporting one of the top pharmaceutical companies in the world. The Oncology 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 : United States (PST, MST, CST) and Canada

Responsibilities for the Oncology 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 Oncology 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 Oncology Clinical Research Associate :

• Salary : $100,000 - $140,000
• Comprehensive Benefits : Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 5 / 2 / 2025. Applications for this job will be accepted for at least 30 days from the posting date.