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Responsibilities:
- Manage one or more global clinical trials from inception to closure, providing study-level oversight and leadership.
- Oversee vendors, recruitment strategies, and study systems such as CTMS and eTMF to ensure quality and inspection readiness.
- Drive risk identification and mitigation, support global submissions, and provide training to stakeholders.
Qualifications:
- Bachelor’s degree plus at least 4 years of progressive pharma or clinical research experience required.
- Strong analytical, communication, and organizational skills with proficiency in business English.
- Experienced in EDC, IRT, CTMS, and eTMF systems and applying ICH/GCP regulations.
Benefits:
- Comprehensive package includes paid time off, medical/dental/vision insurance, and 401(k).
- Eligible to participate in short-term incentive programs.
- Equal opportunity employer committed to integrity and innovation.
AbbVie
AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and Allergan Aesthetics. They are a global, science-driven pharmaceutical company committed to integrity, innovation, and serving the community.