Clinical Research Associate II - Oncology - Remote

Overview

The Clinical Research Associate II (CRA II) plays a crucial role in advancing AbbVie's clinical research efforts, particularly in oncology, by ensuring the successful conduct of clinical trials and maintaining high standards of data integrity and compliance.

In Short

• Primary contact for investigative sites, providing essential information on clinical trials.
• Aligns and trains site staff and principal investigators on trial goals.
• Conducts site evaluations and monitoring activities in compliance with regulations.
• Customizes site engagement strategies based on local insights.
• Mentors less experienced CRAs and supports their development.
• Monitors site activities to ensure patient safety and study performance.
• Ensures quality and timely data submission from study sites.
• Maintains audit readiness at assigned clinical sites.
• Responsible for investigator payments as per contracts.
• Participates in global/local initiatives as assigned.

Requirements

• Minimum of 1 year of clinically related experience, including 6 months in clinical research monitoring.
• Familiarity with risk-based monitoring approaches.
• Preferred qualifications include a tertiary qualification in health-related disciplines.
• Knowledge of oncology and ability to apply scientific concepts to clinical trials.
• Strong planning, organizational, and collaboration skills.
• Ability to leverage technology for customer-centric support.
• Excellent communication skills for establishing site relationships.
• Self-motivated and focused on delivering quality outcomes.

Benefits

• Comprehensive benefits package including paid time off and insurance.
• Eligibility for short-term and long-term incentive programs.
• Opportunity to work in a dynamic and innovative environment.