The Scientist PK is responsible for monitoring of non-clinical PK/TK studies conducted internally and externally both in a GLP and non-GLP environment and support modelling activities.
Requirements
- Design, oversee, and interpret nonclinical PK/QSP studies (GLP and non-GLP) to support regulatory submissions and drug development.
- Conduct PK, PBPK, QSP modelling and/or work with external collaborators.
- Prepare and review regulatory nonclinical submission documents.
- Collaborate with internal stakeholders including pharmacology, toxicology, clinical, regulatory, and CMC teams.
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Visa Sponsorship
- Four Day Work Week
- Generous Parental Leave
- Tuition Reimbursement
- Relocation Assistance