Assoc RA officer (R1122705) in Beijing, China at IQVIA™

Date Posted: 3/24/2020

Job Snapshot

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Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Essential Functions
• Creates an inventory of appropriate regulatory documents based on checklists prepared by Regulatory personnel.
• Identifies project needs, tracks project timelines and implements client requests, with senior review.
• Reviews documents for regulatory completeness, consistency and accuracy, interacts with project team members to assure
completeness, as necessary.
• With oversight may draft text for straightforward regulatory documents, and conduct QC review of documents prepared by the
regulatory unit, project team or client.
• Takes responsibility for managing day-to-day workload for assigned tasks, in collaboration with senior staff.
• May work independently with internal clients and may interact with external clients, under guidance of senior staff.
• Assists with project budget, project management, business development activities and other tasks as required by senior
Regulatory team members.
• May address technical issues with documents and offer assistance to staff.
• Performs other tasks or assignments, as delegated by Regulatory management.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1122705