Medical Director Consultant

🔥 19 minutes ago

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Edison Scientific

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2025

🤖 Artificial Intelligence

🧬 Biotechnology

☁️ SaaS

Artificial Intelligence • Biotechnology • SaaS

Edison Scientific is an AI-driven R&D platform company that builds Kosmos — an "AI Scientist" designed to accelerate biopharma drug discovery and development. The company combines machine learning, domain-specific agents, and embedded scientific expertise to read literature, analyze experimental data, generate and test hypotheses, and execute scientific workflows across the full drug development lifecycle. Edison provides enterprise-ready, on‑prem deployments (SOC2 Type II compliant), custom world models built on proprietary data, and forward‑deployed scientists to partner with biopharma and academic research teams. They highlight partnerships with organizations such as Incyte Corporation and Population Health Partners and have published benchmarks and research tools (e. g. , ChemCrow, PaperQA, Aviary, Robin).

📋 Description

• Knowledge sharing about "day-in-the-life" as an expert working with data in these domains to assemble regulatory submissions. • Describing common tasks or problems where AI could be of value in your workflows. • Identify + describe internal pharma systems that are commonly used for standard workflows. • Generate or review reference ground-truth artifacts to evaluate against - reports, data files, modules, etc. • Identify + add realistic sources of variance or data corruption in study data. • Identify and correct discrepancies in data quality.

🎯 Requirements

• 15+ years of experience within the pharmaceutical/biotechnology industry, ideally with a sponsor. • Doctor of Medicine (MD) required. Board certification preferred. • Experience within Oncology therapeutic area is preferred. • Experience leading or significantly contributing to clinical study protocol design, including endpoint selection and study design rationale. • Strong working knowledge of clinical trial methodology across Phase I–IV studies. • Experience collaborating cross-functionally with biostatistics, clinical operations, regulatory affairs, and data management teams. • Experience serving as Medical Monitor, including safety oversight and clinical data review. • Experience with protocol amendments and lifecycle management of clinical trial documents.

🏖️ Benefits

• Competitive salary and equity • Full healthcare coverage; we pay 100% of premiums for you and your dependents • Support for growing families, including a yearly new parent stipend and fertility coverage through Carrot • Mental health support through Rula, our in-network therapist and psychiatrist network with fast availability • 12 weeks of paid parental leave for maternity, paternity, and adoption • Pet care support with a yearly employer-funded stipend for your animal companions • Commuter benefits so you can pay for transit and parking with pre-tax dollars • 401(k) company matching • $300 health and wellness benefit quarterly • Lunch is on us every day you're in the office, and dinner is on us when you're working late • Regular team off-sites and company events