Promotional Review Board Associate
$70.4k - $123.2kNovo Nordisk US Bio Production Inc.
About The Department Our Marketing & Patient Solutions group creates and delivers human-centered experiences, where innovation meets customer‑centricity, driving the ultimate experience for our patients. Our focus extends beyond transactions to craft experiences as one fully integrated, aligned and connected organization that puts empathy at the center, powered by insight and foresight. We develop an end‑to‑end approach to strategy, focusing on every touchpoint that impacts our customers. We leverage data and insights to inform our decision‑making processes, ensuring that our strategies are rooted in a deep understanding of customer needs and behaviors. Our ‘test and learn’ mindset and approach enables us to iterate rapidly and refine our strategies based on real‑world results. We are building an intentional team culture that is made up of diverse skillsets, united by the shared belief that reinvention and learning is what fuels continuous growth. Do you get excited about exploring the unknown? Does the idea of driving value through human-centered design pull you in? Are you ready to experiment with us? The Position This position has the responsibility of working with the Manager of Marketing Operations along with brand marketing teams and other key functional areas of the organization in the planning, submission, review and finalization of approved promotional marketing materials. The PRB Specialist will provide guidance in all stages in the PRB Process to all stakeholders. The PRB Specialist collaborates with the Managers of Marketing Operations on the planning/scheduling of PRB meetings and any expedited handling of submissions as well as with the Production & Distribution (P&D) Specialists on production and dissemination of materials to the field force and outside parties. He/she also assures quality control of all submissions from and to the agencies and reviewers and scribes notes/captures outcomes in PRB meetings. Relationships Reports to a manager in Marketing Operations. Primary interaction is with all levels within the primary focus areas including, but not limited to, Diabetes, Obesity and BioPharm Marketing, with primary focus on teams that submit into PRB (e.g. Brand teams, Centers of Excellence, Corporate Communications, etc.) on PRB process and workflow. Also interacts with Sales, Medical, Regulatory, and Legal. Also, he/she will work with the Production & Distribution (P&D) Specialists on the distribution of promotional materials. Externally, interacts with agencies/vendors. Works closely with other PRB Specialists. Essential Functions Distribution & Inventory Management: Collaborates with P&D team for all marketing materials being produced through Marketing Operations Knowledgeable about all Marketing materials (reviewed in PRB) that need production (whether executed by Marketing Operations or direct through Marketing Teams/Agencies) Works with P&D Specialists as well as Advocates from his/her assigned brand or launch team to ensure that stock is at correct levels, items are reordered as needed, 24‑month re‑reviews are planned, inventory reports are disseminated and decisions are communicated to Production/Distribution colleagues, as needed Works with P&D Specialists on Inventory management (e.g., reorders, clean‑outs, report dissemination) Finalization And Production Verification: Collaborates with P&D Specialists to manage and file Final Production Verification timing for all marketing materials reviewed in PRB Demonstrates competencies in the technical, regulatory, legal, or other terminology specific to the appropriate functional processes Manages finalization for all materials; FDA 2253 – prepares packages for Regulatory Operations & ensures final production verification is enclosed and non‑FDA – ensures that final production verification is completed Manages finalization for all materials – branded or non‑branded Non‑FDA – ensures that final production verification is completed PRB Review Process Guidance: Proactively provides process and/or system guidance to all stakeholders, including Advocates, Reviewers, Agencies, Regulatory Operations and other operational teammates Shares PRB Planning knowledge/experience with other PRB Specialists when needed PRB Review Process: Assures compliance to the PRB policies and procedures Contributes to the continual improvement of the process and consistency to meet the needs of the marketing teams and reviewers May coordinate and participate in agency status calls to monitor and track status of tactics, as needed Coordinates with Managers of Marketing Operations for PRB Agendas Creates PRB meeting agendas Interacts with internal groups to assure stakeholders are aware of project status and issues for resolution. Responsible for following up with advocates on outstanding submissions of open projects Knowledgeable about all materials coming into PRB via the PRB Submission Plan Maintains all workflow files and archives them upon completion of the job Manages the daily activities related to all promotional materials flowing through the PRB process receipt of submissions from agencies, suppliers, and internal associates, triage/checking of submissions prior to next steps in process, assignment of PRB tracking numbers, tracking status of each submission, routing of all materials to reviewers, and ensuring competition of workflow for each item May provides training to associates and suppliers on the related SOPs, system and/or procedures Quality checks submissions to assure compliance with the established standards and interacts with external and internal submitters to rectify any discrepancies PRB Review Meetings: Primary scribe/note taker for PRB meetings; tracks discussions via notes within jobs for proper updating Collaborates with Editorial colleagues on his/her comments prior to PRB meetings; ensures clarity of changes needed for Editors to perform check changes Physical Requirements 0‑10% overnight travel required. Qualifications A bachelor's degree required; equivalent relevant experience may be substituted where appropriate A minimum 3 years of experience in the development and management of marketing materials in the pharmaceutical industry or equivalent relevant experience Leadership, communication, change management, influencing, and networking skills are critical. Ensures timely execution and follow‑up Must be deadline oriented and able to handle multiple tasks. Must be highly organized and attentive to details Must be attentive and able to follow discussions within meetings and capture outcomes Meeting facilitation experience desired Must be skilled at identifying critical events in the process and interacting with agencies, suppliers, marketing and other business functions in communicating and resolving issues. Anticipates problems and roadblocks to avoid crisis management Planning, execution and follow‑up: Effectively prioritizes and spends his/her time and the time of others on what is important The base compensation range for this position is $70,400 to $123,200. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance. Novo Nordisk offers long‑term incentive compensation and or company vehicles depending on the position’s level or other company factors. Employees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance. The Company also offers time off pursuant to its sick time policy, flex‑able vacation policy, and parental leave policy. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk, we’re not chasing quick fixes – we’re creating lasting change for long‑term health. For over 100 years, we’ve been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what’s possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we’re making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today. Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations. If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at View phone number on click.appcast.io. This contact is for accommodation requests only and cannot be used to inquire about the status of applications. #J-18808-Ljbffr Novo Nordisk
$70.4k - $123.2k
...areas of the organization in the planning, submission, review and finalization of approved promotional marketing materials. The PRB Specialist will provide... ...submissions from agencies, suppliers, and internal associates, triage/checking of submissions prior to next steps...SuggestedLocal areaFlexible hoursNight shift- ...Specialist to collaborate with Marketing Operations, brand teams, and external partners in planning, submitting, reviewing, and finalizing approved promotional materials. The role guides stakeholders through the PRB process, coordinates meetings, and ensures quality...Suggested
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$55k - $70k
...Participate in EMPQ, cleanroom validation, and associated activities/documents. Responsible for... ..., Gas Testing, Gram Staining, Growth Promotion, Bioburden, Gowning Qualifications and... ...documentation, by way of authoring, reviewing and/or approving GMP documents, such as...Work experience placement
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