Senior Clinical Research Associate - Freelance - Remote

Overview

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

In Short

• Performing data verification of source documents.
• Conducting site visits, including pre-study, initiation, monitoring, and termination.
• Confirming adherence to all FDA, ICH-GCP, and local regulations.
• Ensuring implementation and compliance with FDA and ICH-GCP guidelines.
• Participating in budget negotiation and follow-up where applicable.
• Assisting with data validation and query resolution.
• Mentoring junior team members as required.
• Ensuring the completion and collection of regulatory documents.

Requirements

• A minimum of 2 years of monitoring experience in oncology trials.
• Experience monitoring in early-phase trials will be valued.
• Completion of a science-related Bachelor’s degree.
• Excellent knowledge of medical terminology and clinical monitoring process.
• Strong ICH-GCPs knowledge.
• Experience with clinical trial information systems.
• Ability to travel up to 60% on average.
• Bilingualism (English/Spanish) is required.

Benefits

• Opportunity to work in a global organization.
• Engagement in innovative cancer research.
• Flexible working hours.
• Collaborative team environment.
• Professional development opportunities.