Lead, Clinical Pharmacology & MIDD Strategy

Pfizer; Cambridge (MA); Hybrid; USD 106,000 - 177,000; Full time

Benefits offered by this job

Employee Referral Bonus

Hybrid work arrangement

Job summary

Pfizer is seeking a Clinical Pharmacology Lead to support the End-to-End Internal Medicine portfolio. You will provide clinical pharmacology and MIDD input to project teams and regulatory interactions, using PK/PD, modeling, and patient data to guide development strategies and dosing decisions.

The role emphasizes collaboration in a global team, design of robust pharmacology plans, and contribution to regulatory submissions. Hybrid work with on-site requirements is expected in the US.

Qualifications

• Strong quantitative skills with PK/PD modeling and modeling methods.
• MD/PhD or equivalent training in pharmacokinetics/pharmacometrics or related discipline.
• 0+ years of industry experience.
• Pharm D. or equivalent training/experience in pharmacokinetics/pharmacometrics.
• 2+ years of industry experience.
• Excellent written and verbal communication skills.
• Demonstrated presentation skills.
• Ability to work in global team meetings across different time zones.

Responsibilities

• Act as Clinical Pharmacology representative on various team levels.
• Provide expertise, leadership, and deliverables for assigned projects.
• Design and execute clinical pharmacology plans with best practices.
• Coordinate PK/PD analyses and modeling to support dosing decisions.
• Oversee study level activities including protocol authoring and reporting.
• Ensure dose-range finding strategies lead to optimal regimens.
• Contribute to regulatory documents with End-to-End pharmacology input.
• Stay updated with literature and regulatory guidelines.

Skills

PK/PD modeling

Clinical pharmacology

Regulatory interactions

NONMEM

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Education

MD/PhD or equivalent

Pharm D. or equivalent

Tools

NONMEM

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Job description

Pfizer is seeking a Clinical Pharmacology Lead to support the End-to-End Internal Medicine portfolio. You will provide clinical pharmacology and MIDD input to project teams and regulatory interactions, using PK/PD, modeling, and patient data to guide development strategies and dosing decisions.

The role emphasizes collaboration in a global team, design of robust pharmacology plans, and contribution to regulatory submissions. Hybrid work with on-site requirements is expected in the US.