Coordinator, Regulatory Affairs US Advertising and Promotion (Office-based)

Us Advertising And Promotion Coordinator

The US Advertising And Promotion Coordinator combines knowledge of the pharmaceutical business landscape to drive the aims and purpose of the U.S. Advertising and Promotion (USAP) department including the Regulatory review of non-promotional materials, providing operational guidance and development of USAP metrics and trends, as well as, creation and maintenance of sharepoint sites and other business platforms. The contribution from this role will directly benefit the USAP area, as well as cross-functional stakeholders including U.S. Commercial and Research and Development areas : Global Medical Affairs, Clinical, and HEOR.

Responsibilities :

• Functions independently in evaluation and negotiation of R&D (MedComms) project related topics with cross-functional stakeholders.
• Provides complete analysis of USAP department metrics, identifying trends and creating periodic reports
• Develops USAP MedComms training and onboarding materials. Trains new MedComms stakeholders on the Regulatory review process.
• Effectively presents key information to appropriate levels of management and stakeholders.
• Uses problem solving skills to separate and combine tasks into efficient workflow, makes good decisions based upon a mixture of analysis, experience, and judgment.
• Responsible for compliance with applicable Corporate and Divisional Policies and Procedures. Create, Manage, and Analyze USAP Sharepoint sites and other business platforms, as the lead super user
• Responsible for the creation of USAP newsletters. Uses and understands Microsoft Office Suite, Teams, Sharepoint and other business-specific software, including Regulatory Information Management (RIM) such as eDocs
• Provide administrative support and project management support for document requests
• Assists with the in-house organization, management and execution of projects and activities undertaken by USAP
• Super User of materials approval systems. Manage meetings as and when required
• Must have a good grasp of project time requirements to be able to meet deadlines, stakeholder expectations, and avoid over commitments. Conducts all business in a professional manner. Confronts issues in a constructive manner at an appropriate organizational level and take ownership of tasks
• Participates in the sharing of information to promote overall efficiency of the department.
• This role will work a hybrid work schedule - 3 days in office & 2 days remotely from the AbbVie Mettawa, IL headquarters.

Significant Work Activities : Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required

Qualifications :

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.