Project Manager, Global Material Review
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Mettawa, IL
- Commercial
- Hybrid
- Full-time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Ensure all promotional materials are reviewed by cross functional teams, medical, regulatory, compliance and others as required by AbbVie policies. Operate within an Always Audit-Ready mindset.
Provide expertise in content reuse, working with brands and agencies to increase AbbVie’s reuse of content, across channels. Influence and teach brand team members about the benefits and importance of content reuse.
- Facilitate Medical/Regulatory meetings that include Marketing representatives to ensure the process runs efficiently resulting in clarification and/or decisions (e.g. concept meetings, elevation meetings, strategy sessions). Consult with OEC and Legal when required.
- Provide expert process guidance/support for all individuals within the approval process. Responsible for working with third party suppliers and advertising agencies during project development, routing projects through the Med/Reg approval process.
- Act as a subject matter expert for Veeva Vault PromoMats; provide training to internal and external users
- Contribute to the development of new content review workflows and processes
- Contribute to content operational process improvement, searching out and recommending opportunities for increased efficiency
- Monitor timelines for material approval as agreed by the Global Materials Review Grid (GRID).
- Work with AbbVie Global personnel to create agenda and schedule concept, collaboration, and review meetings; facilitate concept, collabs, and ad-hoc meetings
- Identify when escalations are needed; communicate concerns or issues to AbbVie leadership in a timely manner
- Collect and organize all guidance, decisions, and next steps from Global Material Review meetings and disseminate to members. Ensure all reviewer comments are implemented within each draft and final material
- Approve the final approved version of the material post-review in the MR system. Confirm assets for the final approved material is included in Veeva.
- Provide solutions and contingency plans
- Drive MLR audit process, provide proactive support
- Lead and/or assist on special projects for the Global Materials Review Process, as needed; communicate with teams to ensure local review compliance
- Manage Affiliate processes as required for local events (meetings, Congresses, etc.), as well as Co-creation processes, including concept reviews
- Provide Affiliates with Veeva Promomats projects details if review is needed.
- Generate and lead best practices for content review and lifecycle management for assigned brands
- Contribute to continuous process improvement through initiatives such as sharing best practices, peer reviews and performance audits
- Measure to MLR process KPIs, drive continuous improvement, efficiency and effectiveness of the process
- Identify opportunities for MLR process automation so there can be increased focus on content
- High School Diploma or GED required. BA degree or equivalent 5+ years business experience within the design or advertising industry, pharmaceutical or healthcare.
- Project Management knowledge required. Knowledge and prior experience in marketing, and communication or advertising agency experience is a plus.
- Strong planning and organizational skills are required to successfully multitask and problem solve in a fast-paced environment
- Ability to understand marketing campaign messaging for assigned brand; recognizes inconsistencies in campaigns and vocalizes to IBT; basic knowledge of brand references and trials. Share and document best practices and lessons learned to enhance overall functional and business success; proactively provides process expertise to internal and external clients
- Knowledge and prior experience with AbbVie products, marketing, and communication or advertising agency experience is a plus.
- Expertise working in Adobe Acrobat; MS Word, MS Excel, MS Powerpoint and MS Project. Possesses ability to learn and adapt to other software tools as necessary.
- Print production knowledge is a plus.
- Minimum 3 years of experience in project management.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at thetime of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographiclocation, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our short-term incentive programs.
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.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
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If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.
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Pay Range: $
78500 - 141000 USD
Where We Work
Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.