Novo Nordisk

Associate Operational Excellence Director - Clinical, Medical, Regulatory Affairs (Plainsboro, NJ, US)

Plainsboro, United States Type not listed
Regulatory Affairs Director

Novo Nordisk is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

About the Department

The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the same beat is our patient centered focus. At Novo Nordisk, you will help patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We’re changing lives for a living. Are you ready to make a difference?

The Position

The Associate Director, CMR Operational Excellence will be responsible for the transformational improvement and strong execution of critical operational processes across CMR such as contracting, budgets, and governmental R&D spend reporting. The ideal candidate will possess a strong financial and operational background and also a proven ability to deliver transformational process improvements via technology implementation and fit-for-purpose process improvement. The candidate will ensure the timely delivery, accuracy, and transparency of the entire CMR GVP/SVP budget and projections to the GVP/SVP of CMR and ensuring alignment with R&D and NNI strategies and strategy execution. The candidate is also responsible for development of, and execution of, a strategy for CMR transformation of business processes, in close collaboration with other initiatives both within NNI and in R&D. As needed, the Assoc Dir, CMR Operational Excellence will be able to cover for enabling operation individual contributors who support individual CMR VP/AVP areas. In fulfilment of these goals, the Assoc Director will need to build strong relationships, communicate clearly, and drive alignment with stakeholders and/or business partners both within CMR and also within NNI and global functions.

Relationships

The Assoc Director reports to the Director, Strategic Support, within CMR. The incumbent works closely with associate directors, directors, VP/AVPs, and other senior leadership across the organization, including Legal, Finance, and other Functions within USO Clinical Development, Medical and Regulatory (CMR) and in global R&D.

Essential Functions

Responsible for developing and implementing transformation of CMR business processes and related resourcing estimates across all CMR VP/AVP areas

As needed, develops executive level communications to support strategic transformation initiatives

Leads or participates in strategic efforts (e.g., annual business planning, scenario planning) on behalf of CMR for the greater NNI or NNA/S organization and aligned to enterprise strategic direction and NN Way.  This can include driving organizational alignment, identifying and mitigating risks and ensuring alignment with overall business unit and enterprise goals

Lead for ensuring budget, contracting, and transparency training for relevant associates throughout CMR, and acts as backup as needed

Lead for any cross-CMR requests for budget or resource summaries or analyses, such as in resource planning or government transparency reporting

Subject matter expert and primary liaison for cross-CMR budget, contract, and resource questions

Works with business partners inside and outside of CMR to ensure resource strategies are being implemented into their responsible VP/AVP area and monitors progress throughout the year. This includes following local and HQ level models, strategies, or initiatives, as required

Responsible for ensuring fit-for-purpose training and processes across CMR for PO creation, contracting, invoice tracking, and invoice discrepancy troubleshooting

Collect and ensure responsibility of CMR LT area resource projections

Facilitate cross-functional collaboration among business operations within CMR and NNI and also globally, partnering across global R&D

As needed, ensures accuracy and transparency of VP/AVP operating budgets by following company budget timelines and by conducting accruals, chargebacks, and reallocations

As needed, primary point of contact for coordinating governmental transparency reporting within CMR

Physical Requirements

0-10% overnight travel required.  We will consider a remote scenario for the right candidate.

Qualifications

Bachelor’s Degree required

Minimum of 10 years experience required, with 2+ years direct experience with business planning or finance or similar

Demonstrated ability to innovate and drive leading edge digital transformation

Demonstrated ability to work in a cross-functional, fast-paced environment

Ability to manage short- and long-term priorities while working with time sensitive deadlines

Excellent communication skills and ability to speak to all levels of an organization

Ability to solve problems and present solutions

Advanced capability in Excel, PowerPoint and Word required; SAP experience is a plus

High level of independence, integrity, and accountability

The base compensation range for this position is $160,000 to $250,000. 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 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

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Job details

Seniority
Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Plainsboro, United States
Employment type
Not listed

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 74 comparable Director Regulatory Affairs roles across 22 biopharma companies.

74Comparable roles tracked
59Currently active
22Companies hiring similar roles
9Countries represented

Salary context

34 of 74 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Peer group range $174,000 – $295,900 (median $244,150)

Where these roles are based

Top locations among the 74 comparable roles

United States48
Ireland8
United Kingdom7
Poland4
China's Mainland2
Spain2

+ 3 more countries

Seniority mix

74 of 74 peers have a known seniority level

Director60
Senior Director12
Principal2

Therapeutic area mix

9 of 74 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology3
Cardiovascular / CVRM2
Respiratory2
Rare Disease1
Neuroscience1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
AbbVie Director
Same function Same seniority Same country

Open in 5 locations

North Chicago, United StatesFlorham Park, United StatesCambridge, United StatesIrvine, United StatesWaltham, United States
60%similar
AbbVie North Chicago, IL Director
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
60%
Director, RA Global Regulatory Strategy
AbbVie · Cambridge, MA · Director
Function Therapeutic area Seniority Country
60%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
60%
Director, Regulatory Affairs Data Standards and Governance
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.