Head, Clinical Pharmacology - Hybrid or Onsite

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’re seeking a Head, Clinical Pharmacology (Sr. Director) – Hybrid or Onsite to lead and execute the clinical pharmacology strategy for programs built on novel biology, driving both high level decisions and the hands on PK/PD, modeling, and assay work essential to the role. This newly created senior leadership position reports directly to the Chief Medical Officer and serves as the company’s key expert in clinical pharmacology, modeling and simulation, and dose optimization. This is a highly visible, impact heavy position where you will own the end to end clinical pharmacology strategy—designing custom assays with Research, driving PK/PD modeling, informing program level decision making, and shaping regulatory interactions for biology that requires true scientific creativity. If you thrive in an environment where your insights directly influence development strategy, this role offers the opportunity to build and lead the function while advancing innovative precision medicine in immunology and inflammation.     RESPONSIBILITIES   Define and implement clinical pharmacology strategies across multiple programs. Lead PK/PD modeling, dose selection, and bioanalytical planning.  Author and review clinical pharmacology sections of protocols, regulatory documents, and submissions. Collaborate with Clinical Development, Research, Regulatory Affairs, Biostatistics, and Clinical Operations to ensure integrated plans. Represent Clinical Pharmacology in governance committees and regulatory interactions. Oversee vendor management for bioanalytical and modeling activities. Ensure adherence to GCP, ICH guidelines, and all applicable regulatory requirements. Other duties as assigned.    EXPERIENCE & QUALIFICATIONS   ·         Advanced degree (PhD, PharmD, or MD) in Clinical Pharmacology or related discipline required. ·         12+ years of experience in clinical pharmacology within the biopharmaceutical industry. ·         Experience with biologics and immunology/inflammation indications strongly preferred ·         Strong understanding of global regulatory requirements for clinical pharmacology. ·         Leadership experience managing cross-functional teams and external vendors.