Mgr, Reg Affairs (R1107555) in Beijing, China at IQVIA™

Date Posted: 2/14/2020

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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.

• Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters, including salary administration.

• Independently handles personnel issues, conflict management, defines goals that increase knowledge and skills of staff, and defines staff expectations, without involvement of senior managers.

• Assists in the coordination of projects and resources, ensuring quality deliverables to customers.

• May contribute to discussions on implementation of business strategy on a regional basis and will set and implement site-specific objectives, as appropriate. Ensures staff have a consistent understanding and positive impression of strategy for regional and global objectives.

• May have financial responsibility and accountability for one or more Regulatory Affairs sites. Undertakes business development activities and monitors growth and performance, as required.

• May undertake risk analysis and manages the outcome as appropriate.

• Builds strong relationships with managers of other operations and acts as a positive ambassador for Regulatory Affairs.

• May act as a Project Manager for a large stand-alone programme, involving several regulatory or technical deliverables and/or region, and/or operation. May provide strategic regulatory and/or technical consultancy on a variety of projects.

• May manage meetings with Regulatory Agencies.

• May write and/or review a complete single service regulatory proposal and defend costs and timelines to clients.

• May plan and deliver workshops or presentations on Regulatory Affairs topics for conferences or publications.

• May be assigned as Reviewer and/or Approver for Regulatory SOPs or cross-functional SOPs owned by other operations.

• May support global regulatory or technical initiatives or act as a regional representative on a cross-functional initiative.

• Performs other duties, as business needs require.

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: R1107555