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Responsibilities:
- Prepares clinical and regulatory documents needed for drug and device development.
- Coordinates review, approval, and quality control of projects.
- Develops knowledge of submission strategies and regulatory requirements.
Qualifications:
- At least 4+ years of bio-pharmaceutical industry experience.
- Bachelor's degree required; scientific discipline preferred.
- Excellent writing and communication skills with knowledge of medical terminology.
Additional Information:
- Compensation includes base pay, short-term incentives, and benefits.
- Benefits include paid time off, medical/dental/vision insurance, and 401(k).
- AbbVie is an equal opportunity employer committed to integrity and innovation.
AbbVie
AbbVie discovers and delivers innovative medicines and solutions for serious health issues across immunology, oncology, neuroscience, and aesthetics. The company is a global biopharmaceutical leader with a strong focus on research and development, employing thousands worldwide.