SystImmune
Senior Manager/Associate Director, Clinical Pharmacology
SystImmune, Redmond, Washington, United States, 98052
Redmond, WA
Company Overview: SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. Our mission is to revolutionize cancer treatment by developing breakthrough therapeutic multi-specific antibodies and ADCs. With eight assets in ongoing clinical trials and a robust preclinical pipeline, we are committed to advancing innovative therapies from discovery through IND-enabling stages.
Summary: We are 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 contribute 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 (INDs, NDAs, etc.), and respond 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 modeling and simulation activities (NCA, population modeling, exposure-response analyses, etc.).
Familiarity 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.
Minimum 1 - 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 stable, well-funded biotech company with a bright future. 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 including: 100% paid employee premiums for medical/dental/vision, STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
SystImmune is an Equal Opportunity Employer. Interested applicants should send their CV and cover letter to
hr@systimmune.com
#J-18808-Ljbffr
Company Overview: SystImmune Inc. is a dynamic clinical-stage bio-pharmaceutical company headquartered in Redmond, WA. Our mission is to revolutionize cancer treatment by developing breakthrough therapeutic multi-specific antibodies and ADCs. With eight assets in ongoing clinical trials and a robust preclinical pipeline, we are committed to advancing innovative therapies from discovery through IND-enabling stages.
Summary: We are 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 contribute 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 (INDs, NDAs, etc.), and respond 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 modeling and simulation activities (NCA, population modeling, exposure-response analyses, etc.).
Familiarity 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.
Minimum 1 - 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 stable, well-funded biotech company with a bright future. 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 including: 100% paid employee premiums for medical/dental/vision, STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
SystImmune is an Equal Opportunity Employer. Interested applicants should send their CV and cover letter to
hr@systimmune.com
#J-18808-Ljbffr