Oncology Clinical Research Associate (CRA)

Responsibilities

• 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

• At least 3 years of experience as an On-site CRA.
• Comfortable with up to 70% travel (2-3 days per week).
• Valid driver’s license.
• 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).

Pay

Salary: $120,000 - $135,000

Benefits

• Medical
• Dental
• Vision
• 401K
• PTO
• Sick Leave as required by law
• Holidays