Associate Director, Quantitative Pharmacology and Pharmacometrics Cardiometabolic and Ophthalmi[...]

MSD; Rahway (NJ); Hybrid; USD 153,000 - 243,000; Full time

Job summary

An established industry player is seeking an Associate Director for their Quantitative Pharmacology and Pharmacometrics Department. This role offers a unique opportunity to influence the clinical development of novel therapeutic agents for cardiometabolic and ophthalmologic diseases. You will work collaboratively with experienced scientists, leveraging quantitative analyses to optimize drug discovery and development processes. This innovative firm provides a supportive environment for career growth, making it an exciting opportunity for those passionate about advancing healthcare through science and technology. Join a team committed to making a meaningful impact in the biopharmaceutical field.

Benefits

Health care benefits

Retirement benefits

Paid holidays

Vacation days

Sick days

Bonus eligibility

Long term incentive

Qualifications

• Ph.D. with 4+ years or equivalent experience in drug development.
• Experience in population PK/PKPD analyses using pharmacometrics software.

Responsibilities

• Develop model-based strategies for drug discovery and development.
• Collaborate with teams to drive development of cardiometabolic and ophthalmology programs.

Skills

Population PK/PKPD analyses

Interdisciplinary collaboration

Problem scoping and planning

Modeling of complex therapeutics

Communication skills

Education

Ph.D. or equivalent

PharmD or equivalent

MS or equivalent

Tools

NONMEM

Monolix

Phoenix

Job description

Job Description

The Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's Research Laboratories in West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology pipelines.

As an Associate Director, you will represent QP2 on cross-functional teams of experienced scientists to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and ophthalmologic diseases. You will work on the discovery and development of small molecules, biologics and non-traditional therapeutics like peptides, novel biological constructs, and others. The Associate Director is a skilled quantitative drug developer, with a strong, integrated understanding of the strategic elements of drug discovery and development. The Associate Director should demonstrate collaborative work spirit and excellent communication skills and should work independently with minimal supervision.

Within QP2, you have a unique opportunity to accelerate your professional career as a quantitative drug developer taking advantage of our end-to-end pipeline support in one of the world’s most research-intensive biopharmaceutical companies.

Responsibilities:

• Develop model-based strategies (translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within and across development programs and/or departments, to inform and optimize drug discovery and all phases of drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions.
• Represent QP2 on cardiometabolic and ophthalmology discovery, early clinical development and late clinical development teams, leveraging quantitative approaches to drive streamlined development of programs within our growing ophthalmology portfolio.
• Collaborate with other functional areas, as well as with external vendors and partners, creating an aligned, quantitative and model-informed regulatory framework to impact strategies and decisions of drug discovery and development teams.
• Collaborate with other functional areas, as well as with external vendors and partners, on activities related to study design, protocol development, study execution, reporting and interpretation of data.
• Maintain a comprehensive understanding of global regulatory expectations and shape, present and defend regulatory documents and submissions.
• Work closely with pharmacometrics team members and provide input related to analysis and reporting of modeling activities.

Required:

• A Ph.D. or equivalent degree with at least 4 years of experience OR a PharmD or equivalent degree with at least 6 years of experience OR an MS or equivalent degree with at least 8 years of experience, where “experience” means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development, regulatory agency, or academia.
• Educational background in biopharmaceutics, pharmaceutical sciences, pharmacometrics, chemical/biomedical engineering, or a related field.
• Experience in performing population PK/PKPD analyses using standard pharmacometrics software (e.g. NONMEM, Monolix, Phoenix, etc.)
• Proficiency in written and verbal communication, interdisciplinary collaboration, and problem scoping and planning.
• Knowledge in modeling of complex therapeutics.

Preferred:

• Knowledge in cardiometabolic and/or ophthalmology clinical drug development programs
• Expert skills in experimental design, mathematical problem solving, critical data analysis/interpretation, and statistics.
• Scientific understanding of biopharmaceutical and ADME properties of small molecules and/or biologics
• An exemplary record of increasing responsibility, independence, and demonstrated impact in driving drug development decisions through application of model-based approaches.

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.

Expected US salary range:

$153,800.00 - $242,200.00

Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days.

Employee Status: Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements: Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Business Intelligence (BI), Database Design, Data Engineering, Data Modeling, Data Science, Data Visualization, Machine Learning, Software Development, Stakeholder Relationship Management, Waterfall Model

Preferred Skills:

Job Posting End Date: 05/2/2025

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.