Sr. Scientist, Clinical Pharmacology

COMPANY INTRODUCTION

Triveni Bio is breaking new ground in the identification of novel disease targets – working at the convergence of human genetics, best-in-class antibody design, and precision medicine. We are pioneering a Mendelian genetics-informed precision medicine approach to develop functional antibodies for the treatment of immunological and inflammatory (I&I) disorders. Our lead antibody program (TRIV-509) targets kallikreins 5 and 7 (KLK5/7) to directly impact skin barrier function, inflammation, and itch – providing a meaningful and much needed potential treatment option for patients with atopic dermatitis and other barrier disorders. In all the work we do, we adhere to our core values: patient impact, bold and rigorous science, open collaboration, kindness & respect.

SUMMARY

We are seeking a motivated, detail-oriented Senior Scientist to join our Clinical Pharmacology team. In this hands-on role, you will contribute directly to data analysis, modeling, and operational tracking across our clinical-stage and pipeline programs. Working closely with cross-functional teams, you will perform non-compartmental analyses (NCA), population PK/PD modeling, help define and implement bioanalytical strategies, manage bioanalytical data, and actively participate in clinical study team meetings. This is an exciting opportunity for an early-career scientist with 2–3 years of experience looking to expand their skills in hands-on quantitative clinical pharmacology and biologic drug development. Reporting into the Exec. Director, Clinical Pharmacology, and working closely with Clinical Development, Translational Medicine, Biometrics, Regulatory Affairs, and external partners, the Senior Scientist will help generate data and insights that inform dose selection, study design, and key development decisions.

RESPONSIBILITIES

Support the development and implementation of clinical pharmacology plans for clinical development programs

Contribute to the design of PK, PD, biomarker, immunogenicity, and exposure-response assessments in clinical studies

Perform Non-Compartmental Analysis (NCA) using standard software (e.g., Monolix or R) to support clinical study.

Execute data assembly, dataset generation, and preliminary quantitative analyses for Population PK/PD (popPK/PD) and exposure-response modeling using R, Monolix, or equivalent platforms.

Generate high-quality graphical visualizations and summary tables of clinical PK/PD for internal study team updates.

Attend and participate in cross-functional clinical study team meetings, representing the Clinical Pharmacology function.

Collaborate with internal teams and external vendors to ensure timely execution of clinical pharmacology analyses and deliverables

Assist in the preparation and review of clinical study protocols, statistical analysis plans, clinical study reports, and other development documents

Support the preparation of clinical pharmacology components of regulatory submissions and health authority responses

Contribute to model-informed drug development activities and pharmacometric analyses through collaboration with internal and external experts

Present study results and data interpretations to project teams and functional leadership

Maintain knowledge of current scientific, regulatory, and industry trends in clinical pharmacology and pharmacometrics

Other duties as assigned

EXPERIENCE & QUALIFICATIONS

Ph.D. or M.S. in Clinical Pharmacology, Pharmaceutical Sciences, Pharmacometrics, Pharmacokinetics, Biomedical Sciences, or a related scientific discipline

2+ years (Ph.D.) or 5+ years (M.S.) years of relevant industry experience in biotechnology, pharmaceutical, or CRO environments; postdoctoral experience may be considered

Proficiency with R for data manipulation, statistical reporting, and data visualization. Hands-on experience or academic exposure to pharmacometric platforms such as Monolix, or NONMEM.

Experience supporting clinical development programs, preferably involving biologics, antibodies, or immunology/inflammation therapeutics

Knowledge of PK, PD, exposure-response relationships, immunogenicity assessments, and clinical pharmacology principles

Experience working with external CROs and bioanalytical laboratories

Strong scientific communication and data presentation skills

Experience contributing to regulatory documentation is preferred

Ability to travel up to 10% as needed