Associate Director, Nonclinical Project Management - Small Molecules

Novo Nordisk; Måløv; Sur place; DKK 847 000 - 1 245 000; Plein temps

Résumé du poste

Novo Nordisk in Måløv seeks an Associate Director, Nonclinical Project Management for small-molecule programmes from lead candidate selection through clinical development and regulatory submission.

You will lead cross-functional teams, coordinate toxicology, safety pharmacology, drug metabolism and pharmacokinetics, and establish integrated project plans with timelines, budgets and deliverables to drive milestones.

Qualifications

• Academic degree in veterinary medicine, pharmacology, toxicology, pharmaceutical sciences or another life-science discipline.
• Several years of experience in pharmaceutical or biotechnology drug development, including small-molecule development.
• At least three years of nonclinical project management or cross-functional development experience.
• Strong understanding of nonclinical small-molecule development, including DMPK, safety pharmacology and toxicology.
• In-depth knowledge of nonclinical regulatory guidance and expectations.
• Strong planning, prioritisation, risk-management and stakeholder-management skills with excellent English communication.

Responsabilités

• Lead nonclinical project management for a portfolio of small-molecule projects from lead selection through clinical development and market.
• Coordinate work across toxicology, safety pharmacology, drug metabolism and pharmacokinetics, bioanalysis and related development disciplines.
• Establish and maintain integrated project plans covering timelines, budgets, risks, dependencies, resources, and key deliverables.
• Bring teams together to identify and resolve issues, maintain momentum, and prepare projects for important development milestones.
• Drive the preparation of high-quality nonclinical data packages and documentation for regulatory submissions.
• Plan and facilitate nonclinical design reviews and the first Safety Committee Meeting before first human dose trial, supporting regulatory interactions.

Connaissances

Nonclinical PM

Leadership

English comms

Regulatory know-how

Risk management

Formation

Life-science degree

PhD preferred

Description du poste

Department:

Global Discovery & Development Sciences

Location:

Måløv, Denmark

Your impact begins here

You will lead the nonclinical project management of small-molecule programmes from lead candidate selection through clinical development and towards regulatory submission and approval. By connecting scientific disciplines, project priorities and regulatory requirements, you will help teams build robust nonclinical data packages and progress important milestones. Your leadership will create clarity across complex programmes and support their path towards first-in-human studies and beyond.

What you’ll bring

You combine a strong scientific foundation with the ability to bring structure, momentum, and alignment to complex drug-development programmes. You communicate clearly across disciplines and can deliver results through collaboration and influence.

Essential Qualifications Include

• An academic degree in veterinary medicine, pharmacology, toxicology, pharmaceutical sciences or another relevant life-science discipline.
• Several years of experience in pharmaceutical or biotechnology drug development, including experience with small-molecule development.
• At least three years of experience in nonclinical project management or a comparable cross-functional drug development role.
• A strong understanding of nonclinical small-molecule development, including drug metabolism and pharmacokinetics, safety pharmacology and toxicology
• In-depth knowledge of relevant nonclinical regulatory guidance and expectations.
• Strong planning, prioritisation, risk-management and stakeholder-management skills, together with excellent written and verbal communication skills in English.

Useful, but not essential

A PhD in a relevant discipline. Equivalent, relevant industry experience will also be considered.

What you’ll do

• Lead nonclinical project management for a portfolio of small-molecule projects, from lead candidate selection through clinical development and towards market.
• Coordinate work across toxicology, safety pharmacology, drug metabolism and pharmacokinetics, bioanalysis and related development disciplines.
• Establish and maintain integrated project plans covering timelines, budgets, risks, dependencies, resources, and key deliverables.
• Bring teams together to identify and resolve issues, maintain momentum, and prepare projects for important development milestones.
• Drive the preparation of high-quality nonclinical data packages and documentation, including content supporting Investigator’s Brochures and global regulatory submissions.
• Plan and facilitate nonclinical design reviews and the first Safety Committee Meeting before the first human dose trial, while supporting regulatory interactions throughout development.

Who you’ll work with

You will join Nonclinical Project Management within Global Discovery & Development Sciences in Research and Development. The function coordinates nonclinical work across the project lifecycle, from lead candidate selection through clinical development to regulatory submission and approval.

You will work closely with nonclinical development teams, external partners and specialists across toxicology, safety pharmacology, drug metabolism and pharmacokinetics, bioanalysis and related functions. As a key point of contact for nonclinical development, you will also contribute as an integrated member of Global Project Teams or Clinical Development Teams for late-stage projects. Your role will be to connect perspectives, clarify priorities, and help multidisciplinary teams deliver together.

What you can expect here

You can expect a role with broad scientific exposure and responsibility across complex, cross-functional projects. You will have the opportunity to shape how nonclinical programmes are planned and delivered, contribute your expertise to global project decisions, and strengthen your experience across the drug-development lifecycle.

You will work in an environment where curiosity, collaboration, and diverse thinking support long‑term progress in health. You will be trusted to take ownership, make your expertise count, and help teams move forward with clarity.

Salary

Annual Base Salary ranges from 847,000 to 1,245,100 DKK, corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience. The figures are the documented annual minimum and maximum for Job Level 9.

Incentives and Benefits

The salary package may include short‑term and/or long‑term incentives as well as other employee benefits based on position level, location, functional area, and relevant market benchmarks.

Learn more about our Reward Philosophy.

Start now

Your impact begins today. If you are ready to bring scientific disciplines together and lead the delivery of nonclinical small‑molecule programmes, apply for the Associate Director, Nonclinical Project Management – Small Molecules role in Måløv by 23. October 2026.

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