Ophthalmic Clinical Pharmacology: Associate Director

Bausch + Lomb

San Juan (PR)

On-site

USD 130,000 - 200,000

Full time

10 days ago
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Benefits offered by this job

Health insurance
401(k) plan
Tuition reimbursement

Job summary

Bausch + Lomb is seeking a translational scientist to drive nonclinical PK, PK/PD, ADME, clinical pharmacology and pharmacometrics for a robust ophthalmic portfolio. The role spans Rx and consumer lines, requiring leadership across teams and global regulatory interactions.

The candidate will design and oversee PK studies, interpret data, guide go/no-go decisions, and contribute to IND/CTA and NDA/BLA submissions. A PhD with 6+ years’ experience in pharmacology is preferred.

Qualifications

  • PhD in Pharmaceutical Sciences or related field with 6+ years of experience.
  • Experience in PK/PD, pharmacometrics or systems pharmacology; ophthalmic drug development preferred.
  • Strong leadership and cross-functional collaboration skills.

Responsibilities

  • Leads clinical pharmacology, PK, PD, and pharmacometrics across Rx and consumer ophthalmic pipelines.
  • Contributes to study designs, go/no-go decisions, dose selection and life-cycle planning.
  • Provides timelines and deliverables to inform portfolio prioritization.
  • Interacts with other functions to balance time, cost and quality; communicates implications to management.
  • Maintains up-to-date PK/PD methods and software knowledge.

Skills

PK/PD
Pharmacokinetics
Pharmacometrics
Biopharmaceutics
Leadership
Regulatory affairs
Communication
Vendor management

Education

PhD in Pharmaceutical Sciences

Tools

NONMEM
Monolix
Phoenix WinNonlin
R
Simcyp
GastroPlus

Job description

Bausch + Lomb is seeking a translational scientist to drive nonclinical PK, PK/PD, ADME, clinical pharmacology and pharmacometrics for a robust ophthalmic portfolio. The role spans Rx and consumer lines, requiring leadership across teams and global regulatory interactions.

The candidate will design and oversee PK studies, interpret data, guide go/no-go decisions, and contribute to IND/CTA and NDA/BLA submissions. A PhD with 6+ years’ experience in pharmacology is preferred.

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