100 Eli Lilly and Company
100 Eli Lilly and CompanyVerified Source

Senior Advisor Cardiovascular NAMs Investigative Toxicology

126K–205K
Onsite · Indianapolis, Indiana
Posted August 4, 2026
payroll

Overview

We seek a scientist to lead cardiovascular safety NAMs within Investigative Toxicology. This role anchors Lilly’s cardiovascular safety pillar, focusing on in vitro models to assess compound liabilities across cardiac and vascular biology. The ideal candidate will drive mechanistic insights and collaborate across functions to advance translational safety science.

What You'll Do8

  • 1Develop expertise in human-relevant in vitro models for cardiovascular liability assessment, including hiPSC-CMs, hiPSC-ECs, 2D monolayer systems, 3D EHTs, cardiac organoids, and vessel-on-a-chip platforms.
  • 2Design and execute mechanistic investigations into proarrhythmia, QT/AP prolongation, structural cardiomyopathy, mitochondrial cardiotoxicity, DIVI, and endothelial dysfunction.
  • 3Implement electrophysiological and contractile readouts such as MEA recordings, calcium flux imaging, sarcomere assays, and impedance platforms while adopting emerging technologies within the CiPA framework.
  • 4Apply 3D cardiovascular platforms for chronic dosing paradigms to capture structural and vascular injury endpoints beyond electrophysiology alone.
  • 5Serve as primary scientific resource for project teams conducting cardiovascular in vitro studies and coordinate with in silico ADMET Intelligence for integrated decision frameworks.
  • 6Evaluate cardiovascular NAMs technologies like multi-organ liver-heart MPS and AI/ML-assisted imaging, recommending platforms for adoption.
  • 7Act as scientific liaison for CROs and academic partners, overseeing study design, data quality, and deliverables.
  • 8Maintain awareness of regulatory developments, participate in consortia, and publish findings externally.

Requirements11

  • 1PhD in Pharmacology Physiology Biomedical Engineering Toxicology or related field with training in cardiac vascular electrophysiology or biology.
  • 2Advisor (R5): 2+ years postdoctoral or industry experience with advanced cardiovascular in vitro models.
  • 3Senior Advisor (R6): 5+ years postdoctoral or industry experience leading independent scientific contributions and model qualification.
  • 4Hands-on experience with hiPSC-CM differentiation, MEA-based proarrhythmia assessment, 3D EHT functional assessment, or endothelial/vessel-on-a-chip models.
  • 5Ability to design experiments, manage concurrent projects, and prioritize under drug discovery timelines.
  • 6Familiarity with CiPA paradigm ICH S7B/E14 Q&A framework or FDA ISTAND NAMs pathways.
  • 7Strong written and oral communication skills demonstrated through publications or conferences.
  • 8Experience operating in matrixed cross-functional environments.
  • 9Knowledge of high-content imaging AI/ML phenotypic classification or transcriptomic profiling for mechanism-of-injury signatures.
  • 10Exposure to cardio-oncology compound assessment using hiPSC-CM or EHT platforms evaluating electrophysiological and structural/mitochondrial toxicity.
  • 11Mentoring junior scientists or leading embedded scientific activities.

Salary Insight

$126 - $205k per year

Location

Typeonsite
LocationIndianapolis, Indiana

Required Skills

hiPSC-CM differentiationMEA‑based proarrhythmia assessment3D EHT functional assessmentendothelial cell vessel‑on‑a‑chip models
Share:

Similar open positions

Explore active roles that match your skills and interests.

Eli Lilly

4d agoSan Francisco, Californiapayroll

Senior Principal Scientist Discovery Oncology (in vivo Biology) - Lilly

Lead in vivo mouse and rat studies to identify and validate druggable oncology targets while supporting community initiatives. Drive rigorous scientific discovery with autonomy and cross-functional collaboration. Join a purpose-driven team making global impact.

71K–187K
In vivo mouse studiesXenograft modelsSyngeneic models+3 more
1010 Gilead Sciences, Inc.

1010 Gilead Sciences, Inc.

20d agoSan Francisco, Californiapayroll

Senior Scientist Drug Metabolism

Lead advanced PK and PK/PD modeling expertise across discovery and development stages. Drive quantitative DMPK strategy and collaborate with interdisciplinary teams to integrate modeling approaches. Design and validate complex PK/PD and mechanistic models to support dose selection and predict first-in-human exposures. Develop AI-enhanced modeling workflows and partner with CROs to ensure high-quality regulatory submissions. Shape business development and licensing evaluations while participating in cross-functional projects. This role differs by focusing on leadership in culture and driving innovation across scientific domains.

Competitive salary
pythonawsreact+2 more

Eli Lilly

17d agoSan Francisco, Californiapayroll

Scientific Lead Oncology Lilly

Scientific Lead at Lilly Oncology drives discovery oncology initiatives in South San Francisco. You will lead lab-based research to identify druggable targets across small molecules and biologics. This role offers significant career growth within a leading pharmaceutical organization.

126K–205K
pythonawsreact+2 more

1010 Gilead Sciences, Inc.

12d agoSan Francisco, Californiapayroll

Senior Scientist Discovery Sciences Technologies Gilead

We seek a Senior Scientist to advance lipid nanoparticle technology within the LNP Center of Excellence and Discovery Sciences and Technologies department. This role drives innovation in mRNA-LNP therapeutics across virology oncology and inflammation areas. You will collaborate with internal research functions and external partners to translate discoveries into clinical development.

Competitive salary
Lipid ChemistryLNP FormulationIonizable Lipids+10 more

1010 Gilead Sciences, Inc.

5d agoSan Francisco, Californiapayroll

Nonclinical Safety and Pathobiology Lead at Gilead Sciences

We seek a seasoned Nonclinical Safety professional to lead outsourced GLP and non-GLP studies from planning through final report. The ideal candidate combines scientific expertise with operational ownership to deliver inspection-ready outputs. This role drives quality assurance, manages CRO collaborations, and ensures regulatory compliance across discovery and IND-enabling programs. You will shape study timelines, resolve complex issues, and mentor junior staff while championing inclusion and talent development.

147K–190K
ToxicologyPharmacologyGLP+7 more

Organon

21h agoPhiladelphia, Pennsylvaniapayroll

Director Nonclinical Development Organon

Lead nonclinical subject matter expertise for Women’s Health General Medicines and Biosimilars programs. Reports to Executive Director and collaborates with clinical regulatory safety pharmacovigilance chemistry manufacturing and business development. Serves as nonclinical representative on asset development teams and supports regulatory submissions.

152K–259K
Nonclinical toxicologyPharmacologyDMPK+5 more