AbbVie

Study Management Specialist

AbbVie

2 months ago
Seoul, Republic of Korea
Onsite
Full Time
Senior
0 applicants
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AbbVie
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About this role

This role involves managing and leading clinical research projects related to regulatory submissions, study coordination, vendor management, and ensuring compliance with local and international regulations. The position oversees various aspects of study execution from planning to closeout, with a focus on regulatory interactions and project success.

Skills

Qualifications

University degree in a medical/science fieldMinimum 5-year experience in clinical research or industryFluent English
AbbVie

About AbbVie

abbvie.ca

AbbVie is a global biopharmaceutical company (spun out of Abbott in 2013) that discovers, develops and commercializes specialty medicines across immunology, oncology, neuroscience, eye care and virology. It is best known for blockbuster brands such as Humira and a growing portfolio that includes targeted biologics and small molecules (and expanded capabilities after the Allergan acquisition). AbbVie emphasizes large-scale R&D, clinical development and strategic partnerships to advance its pipeline and bring therapies to patients worldwide. Headquartered in North Chicago, Illinois, the company operates globally with a focus on long-term innovation and patient outcomes.

About AbbVie

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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