Medical & Scientific Affairs Advisor

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🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

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Clario

WebsiteLinkedInAll Job Openings

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

• Serve as an imaging advisor supporting company operations and initiatives across assigned therapeutic areas. • Provide scientific input on clinical trial design, image review methodology, and image data quality control. • Manage and enhance processes for independent image review, ensuring consistency, quality, and regulatory readiness. • Monitor, review, and communicate industry trends related to independent review to maintain service leadership. • Implement training standards for new radiologists, study‑specific needs, and emerging imaging criteria. • Contribute to scientific publications, abstracts, editorials, and thought leadership initiatives. • Identify and implement innovations to improve central read efficiency and interpretation techniques. • Create, review, and maintain imaging documentation, including charters, imaging manuals, and study‑specific rules. • Develop operational strategies for new imaging criteria and modalities, including nuclear medicine (e.g., PET/CT). • Support radiopharmaceutical trials, specialized client requests, CMO review processes, sponsor audits, and regulatory inspections. • Partner with application development and business development teams to translate scientific requirements into operational and client‑facing solutions. • Lead, mentor, and develop team members through training, coaching, and performance guidance.

🎯 Requirements

• Bachelor’s degree required; advanced degree preferred, or equivalent practical experience. • 5+ years of experience in clinical trials and/or the pharmaceutical environment. • Demonstrated expertise in multi‑modality imaging projects; medical imaging software experience preferred. • Strong understanding of imaging criteria, clinical trial operations, and regulatory expectations. • Proven ability to lead, mentor, and collaborate across multidisciplinary teams. • Excellent written and verbal communication skills with strong organizational and analytical capabilities. • Ability to work independently and adapt to changing priorities in a fast‑paced environment.

🏖️ Benefits

• Competitive compensation • Comprehensive health, dental, and vision coverage • Retirement savings plan with company contribution • Paid time off and company holidays • Flexible work arrangements (role dependent)