Listed on Moderna’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
Lead sponsor-side oversight of nonclinical studies at Moderna's Canadian operations, managing GLP and non-GLP research from protocol development through final reporting. This role suits experienced study managers and monitors in the biopharmaceutical sector who can manage complex outsourced research programs, work with CROs, and drive regulatory compliance across a matrixed organization.
Our summary, not Moderna’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree in toxicology, pharmacology, or related biological science with 7+ years nonclinical drug development experience, OR Master's with 5+ years, OR PhD with 3+ years
- Sponsor-side study monitor or manager experience with GLP and non-GLP nonclinical studies
- Working knowledge of GLP regulations and global nonclinical regulatory guidance (ICH, FDA, EMA)
- Experience managing CRO partnerships including protocol development, oversight, and report review
- Understanding of end-to-end nonclinical study conduct including protocol development, test article handling, in-life procedures, pharmacokinetic integration, pathology evaluation, and report finalization
- Ability to manage multiple complex studies simultaneously in a matrixed environment
- Strong analytical, organizational, and communication skills with attention to detail
- Ability to influence cross-functional stakeholders without direct authority
- Capacity to work independently in a remote or hybrid environment with sound professional judgment
- Ability to adapt quickly to new data and changing strategic directions