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Clario

Transforming Lives by Unlocking Better Evidence | Decentralized clinical trials | Broadest endpoint technology

Senior Principal Scientific Affairs Advisor – General Medicine, Medical Imaging

Medical AdvisorGeneralFull TimeRemoteSeniorTeam 5,001-10,000Since 1973H1B SponsorCompany SiteLinkedIn

Location

United States

Posted

9 days ago

Salary

0

Seniority

Senior

Bachelor Degree10 yrs expEnglishGoogle Cloud Platform

Job Description

Senior Principal Scientific Affairs Advisor – General Medicine, Medical Imaging

Clario

• 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.

Job 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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