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Purpose:
- Advance AbbVie's pipeline by striving for excellence in clinical research.
- Partner with investigators and site staff for effective trial engagement.
- Focus on site conduct that ensures data integrity, compliance, and performance.
Responsibilities:
- Act as primary point of contact for investigative sites, providing contextual trial information.
- Conduct site evaluation, training, monitoring, and closure activities.
- Manage recruitment techniques and ensure timely, quality data submission from sites.
Qualifications:
- Appropriate tertiary qualification in health-related disciplines preferred.
- Minimum 1 year clinical experience, including 6 months in clinical research monitoring.
- Advanced knowledge of regulatory requirements, ICH/GCP Guidelines, and strong organizational skills.
AbbVie
AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics. A large global biopharmaceutical company, AbbVie fosters a culture of innovation and integrity to transform patients' lives.