CMC Program Development Manager (Boulder, CO, US)

About the Department

The Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics. The CMC team works alongside Quality, Regulatory, Technical Operations and RNAi Early Development professionals at our Boulder, Colorado facility and works closely with our teams in Lexington, Massachusetts.  Together, we are driving change. Are you ready to make a difference.

The Position

Experienced Project Manager that can manage complex projects within budget, on time & within scope. Manage multiple projects simultaneously. Ensure projects are executed & staffed according to project plans. Support Line of Business in developing project roadmap & area master plan. Indirect reporting to CMC Leadership with 1:1, roadblock resolution, risk reporting & overall first level of project guidance.

Relationships

Coached by: Associate Director, CMC Program Development.

Essential Functions

Project Management Lead multi-disciplined project teams to complete projects on-time, on-budget, meeting all requirements (quality, cost, schedule)

Coordinate contract resources & internal resources

Refine & clarify project scope through early project analysis with subject matter experts & owners to further substantiate project purpose

Provide clear goals so that the project secures effective use of time & resources & builds employee motivation

Develop bid packages, bid evaluation & drive vendor selection. Also work with procurement to create project specific contracts

Responsible for financial project accountability through purchase order creation, management, invoicing & cost forecasting

Monitor & control project work with stringent follow-up on quality, schedule & budget so that the project delivers the desired end-product

Responsible for monitoring & reporting project progress, communications to management & other stakeholders & presentation in steering groups

Program Management Lead programs, or series of related projects spanning multiple years, with specific oversight of quality, delivery & cost

Partner with cross-functional teams to visualize project roadmaps (i.e. 1-3 year plan) & master plan (3+ year)

Lead communications for cross-functional stakeholders related to overall project delivery

Indirect Reporting of PMO Staff

Primary communication & escalation path with CMC Leadership via 1:1, board meetings, etc

Ensure the quality/content of steering group status & gate presentations

Use of the PMO tools & standards

Physical Requirements

Percentage of Travel: 10%.

Qualifications

Education: BS degree in a science discipline. Advanced degree in the Life Sciences or related field preferred

Minimum of five (5) years of proven project management experience to include

Minimum of three (3) years of experience in pharmaceutical or biotechnology environment

Advanced project management competencies obtained through relevant project management training or experience

Excellent technical writing & oral communication skills; presentation & facilitation skills; & negotiation & conflict resolution skills

Ability to work in both technical & non-technical areas

Ability to use creativity to resolve problems that arise during project execution

Understanding of product documentation & standard operating procedures

Ability to create & manage work plans & detailed project schedules

Strong analytical/reasoning, organizational & multi-tasking skills

Demonstrated ability to communicate with key stakeholders in a cross-cultural environment & demonstrates superior written & oral communication skills

Develops & maintains strong internal & external relationships

Proficient in basic computer skills including experience with Microsoft Office

Proven project management experience with direct management of multiple projects simultaneously

Proven expertise in planning/organizing, managing execution & revising the work plan for complex problems solved by cross functional teams

Ability to function independently, as well as execution of good judgement in decision making & strong leadership skills

Functions well in team environment

Leadership: Builds strong working relationships. Ability to lead tasks & project teams. Ability to manage a changing work environment with constant changing requirements. Considers PMO standards through enhanced development & continuous improvement

Participative/Supporting/Coaching: Actively participates in team activities, supports ideas/actions of others. Problem solving mindset to resolve issues within influence

Agility: Quickly flexes to changes in responsibilities & business needs with grace & ease

Teaming: Demonstrates behaviours consistent with “for me to win the team must win” beliefs. Collaborates, supports & participates in team activities, with many stakeholders & across functional boundaries to achieve success

Appreciative: Demonstrates appreciative feedback style. Appreciates other team members & their contributions toward assuring the process team wins

Fact Based Decision Making: Demonstrates a disciplined approach to problem solving that is based on data & facts & is consistent with vision/business goals & values

Personally Accountable: Owns the results of individual actions & team’s activities. Models the Novo Nordisk way

The base compensation range for this position is $127,500 to $164,000. 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.

The job posting is anticipated to close on August 17, 2026. The Company may however extend this time-period, in which case the posting will remain available on our careers website at www.novonordisk-us/careers.com.

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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