Clinical Research Associate II

📋 Description

• Primary point of contact for investigative sites; connects stakeholders to sites and strengthens
• Aligns, trains and motivates site staff and PI on goals, protocol and patient treatment principles.
• Conducts site evaluation, training, monitoring activities with GCP/ICH compliance and safety of
• Advances site engagement strategy using CRM tools; reports progress and impact.
• Evaluates protocol and trial requirements to ensure recruitment and retention aligned with patient
• Mentors less experienced CRAs and may participate in global/local task forces.

🎯 Requirements

• Tertiary qualification in health-related disciplines preferred.
• Minimum 1 year clinically related experience; 6 months in clinical research monitoring.
• Knowledge of local regulatory requirements, ICH/GCP guidelines and applicable policies.
• Strong cross-functional collaboration, planning and organizational skills.
• Ability to leverage technology to provide site-centric support.
• Excellent communication, relationship-building and problem-solving skills.

🎁 Benefits

• Equal opportunity employer; US & Puerto Rico accommodations and resources available.