Clinical Research Associate - Oncology

About the Role

Our client is seeking an experienced and highly organized Clinical Research Associate to support their vital Oncology clinical trials. This role will primarily be remote, involving the monitoring and management of study sites to ensure compliance with protocols, regulations, and data integrity. You will play a critical role in advancing cancer treatments by ensuring the smooth and efficient execution of clinical studies, contributing to bringing new therapies to patients more quickly.

Key Responsibilities

• Monitor clinical trial sites to ensure adherence to protocols, SOPs, and regulatory requirements.
• Review and verify case report forms (CRFs) and source documentation for accuracy and completeness.
• Communicate effectively with investigators, study coordinators, and site staff.
• Identify and resolve site-level issues and deviations.
• Prepare monitoring reports and contribute to study documentation.

Requirements

• Bachelor's degree in a life science, nursing, or related field.
• Previous experience as a Clinical Research Associate or in a similar clinical trial role.
• Solid understanding of GCP, FDA regulations, and clinical trial processes.
• Excellent organizational and time management skills.
• Strong communication and interpersonal abilities, with the capacity to work effectively remotely.

Benefits

• Competitive salary and potential for performance bonuses.
• Fully remote working opportunity with travel as needed for site visits.
• Opportunity to contribute to life-saving oncology research.
• Comprehensive health, dental, and vision insurance.
• Professional development opportunities and continued training.