CMC Program Development Manager

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 & teams activities. Models the Novo Nordisk way

The base compensation range for this position is $127500 to $164000. 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 positions 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 -us/.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk were not chasing quick fixes were creating lasting change for long-term health. For over 100 years weve 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 whats possible in healthcare. We embrace diverse perspectives seek out bold ideas and build partnerships rooted in shared purpose. Together were 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-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.