Full-Time

Manager, Material Review and Promotion

Posted on 8/21/2026

AbbVie

AbbVie

10,001+ employees

Global biopharmaceutical company developing medicines

Compensation Overview

$109.5k - $208.5k/yr

+ Long-term incentive program

Florham Park, NJ, USA + 1 more

More locations: Mettawa, IL, USA

Hybrid

Three days in the office per week, Tuesday through Thursday.

Bachelor's

Category
Medical, Clinical & Veterinary (1)
Required Skills
Veeva
Word/Pages/Docs
Marketing
Data Analysis
Excel/Numbers/Sheets

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Requirements
  • The candidate must have 8 or more years of project management or equivalent experience.
  • The candidate must be a subject matter expert in the material review process and associated policies and systems.
  • The candidate must have strong expertise in Veeva.
  • The candidate must have experience in print and digital formats.
  • The candidate must have advanced project management skills and be highly proficient at balancing competing priorities.
  • The candidate must be able to forecast, prioritize, multitask, and manage multiple jobs in a fast-paced, rapidly changing environment.
  • The candidate must be capable of making informed, data-driven decisions under tight deadlines.
  • The candidate must have an advanced understanding of data analytics and measurement.
  • The candidate must be able to quickly learn, adapt to, and comply with business needs, policies, and guidelines.
  • The candidate must have experience in risk mitigation and issue resolution, with the ability to see the big picture.
Responsibilities
  • Facilitate the cross-functional review and approval of advertising, promotional, sales training, and promotional labeling materials.
  • Lead the management of cross-functional team members and advertising agencies.
  • Communicate material status openly with cross-functional team members and advertising agencies.
  • Provide tactical support and oversee project timelines for materials throughout the Material Review Process.
  • Serve as the lead consultant and trainer on the Material Review Process for team members responsible for uploading and approving materials.
  • Review promotional and non-promotional materials through United States Commercial, Medical, Regulatory, and other stakeholder groups.
  • Manage and develop a staff of project managers.
  • Develop solutions and contingency plans to facilitate business success.
  • Hold self and team accountable for results.
  • Mentor and coach others on the Material Review Process.
  • Provide consulting, expertise, and Material Review Process training to cross-functional team members.
  • Evaluate and update processes to adapt to change and optimize efficiency.
  • Coordinate logistics for the timely production, fulfillment, and shipment of materials.
  • Provide leadership for innovative solutions to project hurdles.
  • Develop knowledge of customers' goals and priorities and partner with stakeholders to support those objectives.
  • Lead the review process for promotional and non-promotional materials routed through the Material Review Process.
  • Perform final sign-off on material submissions uploaded into Veeva.
  • Validate that metadata and review tiers align with submitted materials.
  • Determine whether legal/compliance review or an Editorial Quality Check is required.
  • Tag additional reviewers and update the review tier when reviewers are not aligned with the selected tier.
  • Ensure source files are uploaded into Veeva for production vendors.
  • Validate back-end approvals before routing material to Regulatory Affairs for Office of Prescription Drug Promotion submission.
  • Oversee the release of approved material for distribution.
  • Inform inventory vendors when material withdrawal is required.
  • Initiate production of updated package inserts.
  • Identify promotional material requiring inventory updates and initiate the inventory update process.
  • Streamline and simplify internal processes and lead implementation of process changes.
  • Provide guidance and leadership to commercial team members and agencies regarding printing processes.
  • Project-manage a team of 10 to 20 cross-functional team members.
  • Schedule, manage, and facilitate formal concept review requests and live review meetings.
  • Create and communicate weekly review team meeting agendas.
  • Prioritize and schedule additional live meeting requests, including exceptions and revise-and-resubmit meetings.
  • Schedule and facilitate weekly live prioritization meetings with business owners.
  • Review Veeva dashboards to understand upcoming material submission volume.
  • Act as a neutral facilitator in project discussions, summarize team agreements, and maintain documentation of discussion outcomes.
  • Lead discussions on unsuccessful projects to identify learnings and improvement opportunities.
  • Lead team discussions on metrics and evaluate opportunities to improve agility.
  • Attend brand and tactical planning meetings to understand upcoming workload.
  • Send material status notifications through the Material Review Process.
  • Work with Compliance to address identified issues.
  • Notify the Fulfillment Center, business owners, or interactive agencies of material status.
  • Develop, maintain, and track process metrics and communicate results to stakeholders.
  • Provide regular updates on the health of the advertising and promotional review and approval process.
  • Run reports to identify in-market materials affected when an existing piece is updated or changed, and alert business owners.
  • Communicate timely and accurate information and project progress to project owners.
  • Identify project bottlenecks and bring cross-functional team members together to resolve issues.
  • Lead the development of solutions and contingency plans to facilitate business success.
  • Develop best practices and lessons learned and share them with the business.
Desired Qualifications
  • A Bachelor's Degree in Business Management, Science, Education, Communication, or a related field is preferred.
  • Experience in the pharmaceutical industry is preferred.
  • Knowledge and prior experience in marketing, communication, or advertising agency work is preferred.
  • Experience leading or participating in a product launch initiative is preferred.
  • The ability to understand marketing campaign messaging for an assigned brand and recognize inconsistencies in campaigns is preferred.
  • Working knowledge of Adobe Acrobat, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, and Veeva PromoMats is preferred.
  • The ability to learn and adapt to other software tools as necessary is preferred.

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company Size

10,001+

Company Stage

IPO

Headquarters

North Chicago, Illinois

Founded

1888

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Simplify Jobs

Simplify's Take

What believers are saying

  • AbbVie raised 2026 revenue guidance to $67.6 billion after Q2 2026.
  • FDA review of SKYRIZI Crohn's subcutaneous induction targets a late-2026 approval.
  • WCLC 2026 data showed ABBV-1480 90% response in squamous NSCLC.

What critics are saying

  • HUMIRA revenue fell 36.1% in Q2 2026 as biosimilars keep taking share.
  • The Apogee deal cuts 2026 EPS by $0.14 and adds debt financing.
  • Epcoritamab missed the July 23, 2026 DLBCL endpoint, threatening future B-cell franchise growth.

What makes AbbVie unique

  • SKYRIZI and RINVOQ drove $8.8 billion of Q2 2026 immunology revenue.
  • Botox Cosmetic and Juvederm generated $973 million in Q2 2026 aesthetics sales.
  • Apogee purchase adds late-stage IL-13 and TSLP programs for eczema and asthma.

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Benefits

Remote Work Options

Flexible Work Hours

Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

3%

1 year growth

3%

2 year growth

3%
Yahoo Finance
Aug 21st, 2026
AbbVie stock moves independently from market with 0.22 correlation driven by immunology drugs

AbbVie stock shows a correlation of just 0.22 to the S&P 500 over five years, meaning most of its movements stem from company-specific factors rather than broader market trends. The pharmaceutical firm's immunology segment generated nearly $8.8 billion of its $17 billion in second-quarter 2026 revenue, led by SKYRIZI at $5.5 billion and RINVOQ at over $2.5 billion. These treatments for chronic diseases have prices negotiated with payers, not consumers. AbbVie has delivered an annualised return of 21.5% with 23.5% volatility over five years, compared to the S&P 500's 12.9% return at 17.2% volatility. The company converts 28.3% of revenue into free cash flow, nearly double the S&P 500 median of 14.5%.

Grafa
Aug 21st, 2026
AbbVie reports 90% response in lung cancer study.

AbbVie reports 90% response in lung cancer study. * AbbVie reported a 90% objective response rate for ABBV-1480 plus platinum chemotherapy in squamous advanced NSCLC at the selected 10 mg/kg dose. * The same dose produced a 75.9% response rate in non-squamous disease and was selected as the recommended Phase 3 dose. * AbbVie will also present data for Temab-A and ABBV-706 across NSCLC and small cell lung cancer at the 2026 World Conference on Lung Cancer. AbbVie (NYSE:ABBV) reported Phase 1b lung cancer data showing objective response rates of 90% in squamous and 75.9% in non-squamous advanced NSCLC with ABBV-1480 plus platinum chemotherapy. At the 10 mg/kg dose, 27 of 30 patients with squamous disease and 22 of 29 with non-squamous disease achieved objective responses, according to the company. AbbVie said the findings support further evaluation of ABBV-1480 in advanced NSCLC and selected the 10 mg/kg regimen as the recommended Phase 3 dose. The company will present additional clinical results for telisotuzumab adizutecan, or Temab-A, in first-line non-squamous and EGFR-mutated NSCLC at the 2026 World Conference on Lung Cancer. AbbVie will also report ABBV-706 data in relapsed or refractory small cell lung cancer, including new safety analyses covering 240 patients. The company's conference presentations include real-world evidence evaluating SEZ6 as a potential therapeutic target in small cell lung cancer. The updates form part of AbbVie's clinical development program across non-small cell and small cell lung cancers, with several investigational therapies being evaluated across different treatment settings. Frequently asked questions. ABBV signals

Yahoo Finance
Aug 19th, 2026
AbbVie stock eyes breakout as Skyrizi dosing decision could unlock $24.5B revenue growth

AbbVie stock has returned 24.5% over the past three months, trading near its 52-week high. The pharmaceutical company's growth hinges on a pending regulatory decision for SKYRIZI, an immunology treatment that generates nearly a third of guided revenue. SKYRIZI sold $5.5 billion in Q2 2026, up 24% operationally. AbbVie guides the drug to $21.7 billion for 2026 against total company revenue of approximately $67.6 billion. The company has raised its 2026 guidance twice by $600 million combined. A subcutaneous induction option for Crohn's disease awaits regulatory approval this fall. Management expects the new dosing method to meaningfully accelerate SKYRIZI sales, though the commercial impact won't materialise until early 2027 due to contract timelines. Clinical trial results showed endoscopic response and remission rates 25 points above placebo.

BBC
Aug 19th, 2026
UK's Smith+Nephew CFO John Rogers to step down for external role.

UK's Smith+Nephew CFO John Rogers to step down for external role. August 19, 2026 The departure follows Smith+Nephew's decision weeks ago to cut its annual revenue growth forecast after second-quarter sales missed expectations due to weak U.S. knee and hip implant demand and pressure on skin substitute pricing International News via Reuters: Smith+Nephew said on Wednesday its finance chief John Rogers would step down at the end of September to take up an external position in the United States, ending his roughly two-and-a-half-year tenure with the medical products company. Here are some more details: - The departure follows Smith+Nephew's decision weeks ago to cut its annual revenue growth forecast after second-quarter sales missed expectations due to weak U.S. knee and hip implant demand and pressure on skin substitute pricing. - Smith+Nephew said it had appointed Senior Vice President Finance and Group Controller Pierre Palassian as interim chief financial officer until a permanent replacement was appointed. - Palassian, who joined Smith+Nephew in 2017, previously held senior roles at AbbVie and Abbott Laboratories. - Rogers, who took up the CFO role in early 2024, had relocated to the United States in 2025 for operational efficiencies. - Shares in the FTSE 100 company have gained nearly 14% during Rogers' tenure as CFO. - Smith+Nephew said Rogers would receive no severance payment, and that his outstanding incentive and share awards would lapse on September 30 under leaver rules. Reporting by Neeshita Beura in Bengaluru; Editing by Subhranshu Sahu - Advertisement - August 19, 2026 - Advertisement -

Yahoo Finance
Aug 15th, 2026
AbbVie shows strong cash flow margin of 34.8% but faces tepid revenue growth

AbbVie, the biopharmaceutical company spun off from Abbott Laboratories in 2013, has risen 9.7% to $249.64 per share over the past six months. The company generates $64.39 billion in revenue over the past 12 months, benefiting from significant economies of scale in its operations. AbbVie's free cash flow margin averaged 34.8% over the last five years, amongst the best in the healthcare sector. This strong cash generation enables reinvestment and capital returns to investors. However, the company's five-year annualised revenue growth of 3.7% remains tepid compared to sector peers. Despite this weakness, AbbVie's shares trade at 16.3 times forward price-to-earnings ratio. The company develops and markets medications for autoimmune diseases, cancer, neurological disorders, and other complex health conditions.