Senior Clinical Scientist

2 days ago

🍂 Massachusetts – Remote

Although this job is listed in Massachusetts, this company may be open to hiring remote in other states.

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

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PathAI

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PathAI is a leading healthcare technology company dedicated to advancing pathology through the use of artificial intelligence. Their mission is to improve patient outcomes by providing AI-powered technology that offers valuable insights for biomarker discovery and drug development. PathAI collaborates closely with biopharma and pathology laboratories to enhance laboratory workflows and improve diagnostics. Their AI-driven pathology solutions, such as the AISight Digital Pathology Image Management System, are utilized by major laboratories and research centers worldwide, helping to power digital pathology and precision medicine initiatives. PathAI's technology is leveraged by top biopharma companies to transform drug discovery and diagnostics, making significant contributions to the fields of healthcare and biotechnology.

artificial intelligence • pathology • digital pathology • oncology • immuno-oncology

501 - 1000 employees

Founded 2016

🤖 Artificial Intelligence

⚕️ Healthcare Insurance

🧬 Biotechnology

💰 $165M Series C on 2021-05

📋 Description

• PathAI is on a mission to improve patient outcomes with AI-powered pathology. • We are transforming traditional pathology methods into powerful, new technologies. • These innovations in pathology can help accelerate drug development and improve confidence in the accuracy of diagnosis. • At PathAI, you'll work with a diverse and talented team of people, dedicated to solving complex problems and making a huge impact. • As a Senior Clinical Scientist, you will play a key role in driving our in vitro diagnostic (IVD) device projects, strategy, and roadmaps. • This individual will be responsible for activities across the IVD development lifecycle, including development of clinical science plans and clinical study protocols for validation studies. • You'll provide scientific oversight during clinical trials, analyzing study results, and contributing to regulatory submissions.

🎯 Requirements

• Advanced degree (PhD, MD, PharmD, or equivalent) in a relevant scientific discipline such as biomedical sciences, pathology, or clinical research. • 3+ years of experience in clinical development, clinical trials, or regulatory affairs within diagnostics, medical devices, or biotech/pharmaceutical industries. • Experience with regulated IVD development including Class II and Class III devices. • Experience in digital pathology, AI-powered diagnostics, or computational pathology is a plus. Experience with pharmaceutical drug and/or companion diagnostic device development preferred. • Knowledge of clinical trial design, regulatory submission processes, and GCP/GCLP guidelines. • Strong analytical skills and ability to work with biostatisticians to interpret clinical data. • Excellent written and verbal communication skills, with the ability to convey complex scientific concepts to diverse audiences. • Ability to work effectively in a fast-paced, collaborative environment.