Senior Principal Scientific Affairs Advisor – General Medicine, Medical Imaging

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🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

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Logo of Clario

Clario

5001 - 10000 employees

Founded 1973

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 Private Equity Round on 2019-10

Healthcare Insurance • Biotechnology • Artificial Intelligence

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• Provide scientific and medical leadership for gastroenterology therapeutic area of responsibility to internal and external stakeholders. • Collaborate with Business Development to secure new business opportunities and expand market presence. • Serve as a scientific advisor to sponsors regarding imaging strategy and implementation within clinical trials. • Support study teams and internal departments through expert guidance on trial design, image review methodologies, and quality control practices. • Identify and implement innovative tools, technologies, and process improvements to enhance operational effectiveness. • Partner with cross-functional teams to align technology enhancements and service offerings with organizational objectives. • Ensure scientific accuracy, quality, compliance, and integrity across project deliverables. • Support development and review of imaging charters, imaging manuals, review rules, study reports, and other technical documentation. • Gather and document scientific and business requirements from clients and internal stakeholders.

🎯 Requirements

• Bachelor's degree in Life Sciences, Medical Imaging, Medicine, Clinical Research, or a related scientific discipline. • Minimum 10 years of clinical trial experience within a CRO, pharmaceutical, biotechnology, or related research organization. • Extensive experience supporting imaging-based clinical trials. • Experience working within regulated environments, including: GCP GLP ICH Guidelines FDA Regulations ISO Standards 21 CFR Part 11 • Experience in project planning, reporting, financial management, and resource coordination. • Demonstrated scientific research experience and established publication record. • Experience collaborating with cross-functional stakeholders and external sponsors. • Advanced knowledge of clinical research methodologies and medical imaging applications. • Strong understanding of project management and data management principles. • Proficiency with Microsoft Office applications, including Word and Excel.

🏖️ Benefits

• Professional development opportunities • Global team events

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