Associate Director, Content Approval Operations

Novartis AG

East Hanover, NJ

JOB DETAILS
SALARY
$152,600–$283,400 Per Year
SKILLS
Artificial Intelligence (AI), Automation, Biotech and Pharmaceutical, Channel Strategies, Coaching, Continuous Improvement, Cross-Functional, Digital Asset Management Software (DAM), Establish Priorities, FDA Requirements, Forecasting, Leadership, Legal, Library and Information Science, Literacy, Marketing, Marketing Communications, Metadata, Metrics, Operational Communications, Performance Analysis, Performance Management, Process Improvement, Regulations, Reporting Dashboards, Risk Management, Teach Graduate Students, Team Lead/Manager, Traceability, Willing to Travel
LOCATION
East Hanover, NJ
POSTED
29 days ago

#LI-HybridNovartis has an exciting opportunity for an Associate Director, Content Approval Operations, to lead the execution, and continuous improvement of Content Approval Services related to Core Claims, Reference Librarian resources, and Workflow Management Capabilities training Master Teams List. This role has shared accountability for functionally overseeing and setting priorities for the team and ensuring disciplined, compliant, and predictable execution of the Material Approval Process (MAP). The Associate Director acts as an operational anchor and escalation partner, translating strategy into execution, enabling foundational AI & Automation that will reduce risk, effort and unlock team performance, ensuring strong collaboration across Medical, Legal, Regulatory (MLR), Marketing, Agencies, and Operations partners.This position will be based in East Hanover, NJ and will not have the ability to be located remotely. Please note that this role would not provide relocation, and only local candidates will be considered. This position will require up to 5% travel as defined by the business (domestic and or international).Key Responsibilities:Claims & Reference Operations Governance:Partner with Core Claims and Medical teams to ensure compliant creation, governance, and maintenance of claims and reference content aligned to approved standardsOversee end-to-end progression of claims through the Material Approval Process (MAP), ensuring quality, traceability, and metadata accuracyDrive intake discipline, workload prioritization, and forecasting aligned to brand demand and enterprise prioritiesEnsure claims libraries and approved reference repositories remain current, auditable, and enabled for reuseMaterial Approval Process (MAP) Execution & Optimization: Support execution of MAP workflows across brands and functions, ensuring submission readiness, routing accuracy, and review efficiency while monitoring operational performance (throughput, cycle time, quality) and proactively address risks, bottlenecks, and rework driversPartner with the Director to implement process improvements, including AI-assisted capabilities and automation, to enhance compliance and efficiencyPeople Leadership and Matrix Team Oversight:Provide day-to-day functional oversight, prioritization, and coverage planning across Core Claims, References Operations, and Material Approval Enablement teams, including leading, coaching, and developing the teams and serving as a first‑line escalation point for people, delivery, and operational challengesServe as a first-line escalation point for operational, delivery, and team-related challenges, reinforcing governance and standardized ways of working.Lead or co‑lead targeted improvement initiatives that enhance predictability, quality, and user experienceCross-Functional Partnership:Act as a trusted partner across Medical, Legal, Regulatory (MLR), Marketing, Agencies, and Operations, communicating status, risks, and recommendations clearly and proactivelyEssential Requirements:Bachelor's degree required in Business, Marketing, Communications, Information Management, or related discipline; advanced degree preferred5+ years of experience in pharmaceutical marketing operations or pharmaceutical content approval with strong understanding of FDA promotional regulations and MAP/MLR review processesAt least one year of people leadership of direct reports or team lead experienceExperience with content approval and DAM platforms (e.g., Veeva, Aprimo)Proven ability to work with operational metrics, dashboards, and performance dataStrong stakeholder management and cross-functional collaboration skillsAbility to translate strategy into disciplined execution in complex, regulated environmentsFoundational AI literacy with the ability to apply critical thinking and compliance judgmentNovartis Compensation Summary:The salary for this position is expected to range between $152,600 and $283,400 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.Desirable Requirements:Experience integrating AI or automation into operational workflows

About the Company

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Novartis AG

Novartis provides healthcare solutions that improve and extend people’s lives. We use science-based innovation to address some of society’s most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. Our company is focused on industry-leading divisions with innovation power and global scale: pharmaceuticals, eye care and generic medicines Novartis is headquartered in Basel, Switzerland. Novartis Group companies employ approximately 120,000 associates and its products are available in more than 180 countries around the world.

COMPANY SIZE
10,000 employees or more
INDUSTRY
Biotechnology/Pharmaceuticals
FOUNDED
1996