Associate Director, Ophthalmic Clinical Pharmacology

Bausch + Lomb

Montgomery (AL)

On-site

USD 130,000 - 200,000

Full time

12 days ago
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Benefits offered by this job

Medical, dental, vision insurance
401(k) plan with company match
Tuition reimbursement
Paid holidays and well-being benefits

Job summary

Bausch + Lomb in the United States seeks a translational scientist to lead clinical pharmacology and pharmacometrics activities across Rx ophthalmic and consumer eye health programs. The role requires a PhD and 6+ years' experience in PK/PD, PBPK, and modeling, with leadership in project delivery and cross-functional collaboration.

You will design studies, support regulatory filings, and communicate findings to management and external partners while staying current with ICH/FDA guidance.

Qualifications

  • PhD in Pharmaceutical Sciences, Clinical Pharmacology, Pharmacometrics, or related field.
  • 6+ years of relevant experience in PK/PD, pharmacometrics, or systems pharmacology.
  • Ophthalmic drug development or ocular PK experience strongly preferred.

Responsibilities

  • Lead clinical pharmacology, PK/PD and pharmacometrics activities across Rx ophthalmic programs.
  • Design and oversee nonclinical PK and clinical pharmacology studies including first-in-human.
  • Communicate implications to management and support regulatory submissions.
  • Maintain up-to-date knowledge of PK/PD methods and software.

Skills

Leadership PK/PD
Regulatory collaboration
Communication
Vendor management

Education

PhD in Pharmaceutical Sciences

Tools

NONMEM
Monolix
Phoenix WinNonlin
R
GastroPlus
MATLAB

Job description

Bausch + Lomb in the United States seeks a translational scientist to lead clinical pharmacology and pharmacometrics activities across Rx ophthalmic and consumer eye health programs. The role requires a PhD and 6+ years' experience in PK/PD, PBPK, and modeling, with leadership in project delivery and cross-functional collaboration.

You will design studies, support regulatory filings, and communicate findings to management and external partners while staying current with ICH/FDA guidance.

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