Associate Director, Quantitative Clinical Pharmacology

🕒 3 days ago

🇺🇸 United States – Remote

💵 $135k - $175k / year

⏰ Full Time

🟠 Senior

👔 Director

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Simulations Plus, Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 1996

💊 Pharmaceuticals

🧬 Biotechnology

☁️ SaaS

💰 Grant - Simulations Plus on 2024-11

Pharmaceuticals • Biotechnology • SaaS

Simulations Plus, Inc. is a science-driven software and consulting company that provides mechanistic modeling, AI-enabled workflows, and expert services to support model‑informed drug development (MIDD) across discovery, development, clinical operations, and commercialization. Its product suite includes GastroPlus (PBPK/PBBM), MonolixSuite (pharmacometrics), ADMET Predictor (ML for ADMET), DILIsym (quantitative systems toxicology), Thales (QSP), and Pro‑ficiency (learning/simulation), and the company offers consulting, training, regulatory strategy support, and bundled solution packages. Simulations Plus emphasizes mechanistic and AI-enabled tools for ADMET prediction, PBPK, pharmacometrics, QSP/QST and serves pharmaceutical and biotech clients (noting ~30+ years in business, ~280+ clients and use by 19 of the top 20 pharma companies).

📋 Description

• Lead and collaborate with multi-disciplinary teams on quantitative clinical pharmacology projects and programs • Provide clinical pharmacology and pharmacometric consultation to company projects and programs • Support clinical study protocols, study conduct, data analysis, and report writing • Participate in regulatory interactions with health authorities • Provide consulting using PBPK, population PK, PK/PD, exposure-response modeling and simulation, and noncompartmental analyses • Use GastroPlus, MONOLIXSuite, NONMEM, R, or other tools • Apply advanced scientific knowledge to assigned programs and projects • Ensure appropriateness of methods, data integrity, and accuracy of results • Maintain communication between the company and clients throughout project execution • Engage clients regarding strategic approaches, results, regulatory implications, and findings • Build positive, productive, and profitable client relationships • Prepare technical reports, synopses, executive summaries, and regulatory documents • Conduct advanced literature searches and integrate research findings into project methodologies and results • Share findings with internal and external project teams • Prepare abstracts, presentations, and publication-ready manuscripts • Mentor and provide feedback to junior scientists • Participate in cross-divisional scientific strategy discussions • Serve as an expert resource for the Business Development Team • Stay current with relevant scientific literature • Attend and present at conferences, client meetings, and government meetings • Develop and teach GastroPlus, MONOLIX, and other workshops and courses • Perform other duties as assigned

🎯 Requirements

• 6+ years of applied clinical pharmacology experience preferred • 4+ years of leading projects, programs, and scientists preferred • Previous supervision of junior clinical pharmacologists and pharmacometricians, fellows, and students preferred • Strong experience presenting scientific results to professional audiences • Extensive experience preparing, submitting, and receiving approval for publications in scientific journals • Population pharmacokinetic and pharmacokinetic/pharmacodynamic modeling and simulation experience • Non-compartmental and compartmental pharmacokinetics experience • Mechanistic physiologically based pharmacokinetic modeling and simulation experience • Excellent communication, presentation, and leadership skills • Relationship-building skills with the ability to work closely with project leaders and team members • Strong organization skills and ability to handle multiple tasks simultaneously • Ability to handle tight deadlines • Great critical-thinking and problem-solving skills • Some travel required for meetings, conferences and events • PharmD, PhD, or masters in pharmacokinetics, clinical pharmacology, or related field • Advanced clinical pharmacology related training preferred

🏖️ Benefits

• Fully remote work • Flexible schedules • Generous vacation policy • Affordable health coverage • Annual bonus • Employee well-being support • Positive workplace culture