Associate Director, Clinical Pharmacology - Oncology Biotech

SystImmune; Princeton (NJ); On-site; USD 150,000 - 200,000; Full time

Benefits offered by this job

Comprehensive benefits package

Equal Opportunity Employer

Job summary

SystImmune, Inc. is seeking a Senior Manager/Associate Director of Clinical Pharmacology to lead the development and execution of pharmacology strategies for ADC assets in a oncology-focused portfolio.

You will direct PK/PD analyses, dose optimization, and regulatory filings while collaborating with Clinical, Research, Regulatory, and Biometrics teams in Princeton, NJ and nearby sites. The role requires extensive experience in clinical pharmacology, pharmacometrics, and drug interaction

Qualifications

• MS/PharmD/PhD in biology or pharmaceutical sciences with focus on pharmacology and pharmacometrics.
• Understanding of clinical pharmacology study design, data analysis and regulatory requirements.
• Minimum 1–5 years of experience in clinical pharmacology and pharmacometrics with hands-on quantitative analysis.
• Prior experience in ADC development is a plus.

Responsibilities

• Plan and conduct oncology clinical pharmacology studies with complex scope.
• Guide dose, schedule and drug‑drug interaction considerations with cross‑functional colleagues.
• Perform quantitative pharmacology analyses and interpret results across development phases.
• Lead pharmacometrics analyses to support development and address scientific questions.
• Prepare and review clinical pharmacology sections of study protocols, reports, investigators' brochures and regulatory filings.

Skills

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Pharmacometric modelling

MIDD (model-informed drug development)

Data analysis

Education

MS/PharmD/PhD in biological or pharmaceutical sciences

Tools

NONMEM

R

Simcyp

WinNonlin

Job description

Weare seeking a high-quality Senior Manager/Associate Director of Clinical Pharmacology to lead the development and execution of clinical pharmacology strategies for ADC assets. The ideal candidate will provide expertise in pharmacokinetics, dose optimization, pharmacometrics, and drug interaction assessment, collaborate with cross-functional teams (Clinical, Research, Regulatory, Biometrics, etc.), and manage clinical pharmacology studies, data analysis, and regulatory filings.

Essential Duties and Responsibilities:

• Play a pivotal role in planning and conducting cutting-edge oncology clinical pharmacology studies that are of higher complexity both in scope and volume
• Guide dose and schedule determination, dose optimization, and drug-drug interaction issues, collaborating closely with cross functional colleagues
• Perform quantitative pharmacology analyses and contributes to the interpretation of study results through all phases of clinical development
• Perform pharmacometric analyses to support drug development and address scientific questions
• Take a lead role in preparing and meticulously reviewing clinical pharmacology sections of study protocols, reports, investigators' brochures and regulatory filings (IND’s, BLA’s, etc.), and responds to regulatory inquiries related to clinical pharmacology

Required Qualifications:

• Experience with a range of clinical studies including first-in-human, proof-of-concept and registrational studies
• Understanding of drug development, including model informed drug development (MIDD) and the overall pharmaceutical R&D process
• Advanced knowledge and understanding of pharmacokinetics (PK), pharmacodynamics (PD), PK/PD, Exposure-Response (ER), and Quantitative systems pharmacology
• Demonstration of strong quantitative skills, conceptual, technical and hands on development expertise with modelling and simulation activities (NCA, population modelling, exposure-response analyses etc)
• Familiar with analysis software (e.g., NONMEM, R, Simcyp, WinNonlin) along with PK modeling and computer skills in scientific graphing

Education And Experience:

• MS, PharmD, or PhD in biological or pharmaceutical sciences, with a focus on pharmacology and pharmacometrics
• Understanding of clinical pharmacology study design, data analysis, and regulatory requirements
• Minimum1 - 5 years of experience in clinical pharmacology and pharmacometrics, with hands-on experience in quantitative analysis
• Prior experience in the field of ADC development is a plus

The hiring pay range for this position is $150,000 - $200,000 per year based on skills, education, and experience relevant to the role.

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package.

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.