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Medical & Scientific Affairs Advisor

Clario
CLARIO
5+ years
Not Disclosed
Remote, USA, Remote
10 May 7, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical & Scientific Affairs Advisor

Company: Clario (part of Thermo Fisher Scientific)
Location: United States (Remote)
Employment Type: Full-Time


About the Company

Clario develops regulated clinical trial technology and scientific solutions that improve evidence generation and patient outcomes. Its platforms support clinical research, diagnostics, and medical decision-making in highly regulated environments.


Role Overview

The Medical & Scientific Affairs Advisor serves as a scientific and imaging expert supporting clinical trial imaging strategy, regulatory compliance, and innovation in independent image review processes. The role bridges scientific, operational, and business functions to enhance imaging quality and trial efficiency.


Key Responsibilities

Scientific & Imaging Leadership

  • Act as imaging subject matter expert across therapeutic areas

  • Provide input on clinical trial design and imaging methodologies

  • Guide image quality control and review processes

  • Develop operational strategies for imaging criteria and modalities (e.g., PET/CT, nuclear imaging)

Clinical Trial Support

  • Support independent image review processes ensuring consistency and regulatory readiness

  • Assist radiopharmaceutical and imaging-based clinical trials

  • Contribute to sponsor audits and regulatory inspections

  • Support specialized client imaging requests and case evaluations

Documentation & Standards

  • Create and maintain imaging documentation (charters, manuals, study rules)

  • Develop training materials and operational guidelines

  • Implement standardized training for radiologists and imaging teams

Innovation & Process Improvement

  • Identify improvements in central imaging review efficiency

  • Contribute to development of new imaging techniques and workflows

  • Monitor industry trends and emerging imaging technologies

Collaboration & Leadership

  • Partner with business development and application teams

  • Translate scientific requirements into operational solutions

  • Lead, mentor, and train team members

  • Contribute to publications, abstracts, and scientific presentations


Required Qualifications

  • Bachelor’s degree (advanced degree preferred) or equivalent experience

  • Minimum 5+ years of experience in clinical trials or pharmaceutical industry

  • Strong expertise in multi-modality medical imaging

  • Experience with imaging software tools (preferred)

  • Strong understanding of clinical trial operations and regulatory requirements

  • Proven leadership, mentoring, and cross-functional collaboration skills

  • Excellent written and verbal communication skills

  • Strong analytical and organizational abilities

  • Ability to work independently in a fast-paced environment


Preferred Skills

  • Experience in radiology, cardiovascular, or nuclear imaging

  • Exposure to regulatory audits and sponsor interactions

  • Experience in clinical imaging innovation or research publications


Work Environment

  • Remote (United States-based)

  • Flexible work arrangements depending on role requirements

  • Cross-functional global collaboration


Company Values

Clario emphasizes inclusion, innovation, and improving patient outcomes through better clinical evidence. The organization promotes diversity, equal opportunity, and a collaborative work culture focused on scientific impact.