Senior Scientist I - Drug Metabolism
Novo Nordisk
August 07, 2026
On-site
Lexington, MA
Clinical Research and Development
The Senior Scientist, DMPK will provide scientific leadership in the discovery of small molecule drug candidates by integrating DMPK strategy across multiple therapeutic areas.
Responsibilities:
- Lead DMPK strategy for discovery programs, aligning ADME objectives with project milestones.
- Apply fit-for-purpose in silico models, PK/PD, PBPK, and exposure–response to predict human pharmacokinetics/dose and de-risk programs.
- Integrate DMPK data with medicinal chemistry and pharmacology to guide chemical design and prioritize drug-like chemical matter.
- Propose and oversee internal/external research initiatives (study design, data analysis, documentation).
- Manage CRO partners with specialized ADME capabilities (quality, timelines, cost-effectiveness).
- Collaborate with global ADME experts to harmonize methodologies and share best practices.
- Communicate DMPK strategy, findings, and risk assessments to project teams and senior management; contribute to go/no-go decisions.
- Represent the company externally as needed (publications, conferences, scientific consortia).
- Stay current on DMPK methodologies, regulatory expectations, and modeling technologies.
Qualifications:
- BS/BA with 10+ years; or Master’s with 8+ years; or PhD with 4+ years relevant experience.
- Experience designing and conducting ADME research in pre-clinical and/or clinical development.
- Strong ADME expertise; hands-on PK and PK/PD modeling or biotransformation highly desirable.
- Strong pharmacokinetics and drug metabolism knowledge.
- Preferred: DMPK or PK/PD modeling project experience.
- Proficient scientific communication and stakeholder engagement.
Benefits:
- Medical, dental, vision; life and disability insurance; 401(k); flexible spending accounts; employee assistance; tuition reimbursement; voluntary benefits; sick time, flexible vacation, parental leave.
Application instructions:
- For accommodation requests only: call 1-855-411-5290.
Responsibilities:
- Lead DMPK strategy for discovery programs, aligning ADME objectives with project milestones.
- Apply fit-for-purpose in silico models, PK/PD, PBPK, and exposure–response to predict human pharmacokinetics/dose and de-risk programs.
- Integrate DMPK data with medicinal chemistry and pharmacology to guide chemical design and prioritize drug-like chemical matter.
- Propose and oversee internal/external research initiatives (study design, data analysis, documentation).
- Manage CRO partners with specialized ADME capabilities (quality, timelines, cost-effectiveness).
- Collaborate with global ADME experts to harmonize methodologies and share best practices.
- Communicate DMPK strategy, findings, and risk assessments to project teams and senior management; contribute to go/no-go decisions.
- Represent the company externally as needed (publications, conferences, scientific consortia).
- Stay current on DMPK methodologies, regulatory expectations, and modeling technologies.
Qualifications:
- BS/BA with 10+ years; or Master’s with 8+ years; or PhD with 4+ years relevant experience.
- Experience designing and conducting ADME research in pre-clinical and/or clinical development.
- Strong ADME expertise; hands-on PK and PK/PD modeling or biotransformation highly desirable.
- Strong pharmacokinetics and drug metabolism knowledge.
- Preferred: DMPK or PK/PD modeling project experience.
- Proficient scientific communication and stakeholder engagement.
Benefits:
- Medical, dental, vision; life and disability insurance; 401(k); flexible spending accounts; employee assistance; tuition reimbursement; voluntary benefits; sick time, flexible vacation, parental leave.
Application instructions:
- For accommodation requests only: call 1-855-411-5290.