Clinical Research Associate II

📋 Description

• Primary contact for investigative sites; connect stakeholders to sites and strengthen AbbVie’s
• Aligns and motivates site staff and investigators on trial goals, protocol, and patient treatment
• Conducts site evaluation, training, routine and closure monitoring with GCP/ICH/AbbVie SOPs to
• Customize site engagement strategy using CRM tools and report impact of engagement efforts.
• Link protocol, science, and trial requirements to day-to-day execution; optimize recruitment and
• Mentor less experienced CRAs and participate in global/local task forces as assigned.

🎯 Requirements

• Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing)
• Minimum 1 year clinically related experience; at least 6 months in clinical research monitoring
• Knowledge of therapeutic area indications; ability to apply scientific concepts to trials.
• Advanced knowledge of local regulatory/ICH/GCP requirements and AbbVie policies.
• Strong cross-functional collaboration, planning, and organizational skills; able to manage
• Ability to leverage technology and CRM tools to provide site-focused support.

🎁 Benefits

• Comprehensive benefits package including paid time off, medical/dental/vision insurance, and 401(k).
• Eligibility for short-term incentive programs.
• AbbVie's commitment to equal opportunity and a supportive work environment.