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Research Technologist, Medical & Scientific Affairs

External
clarioclinical logoClarioclinical · Remote
Full-timeRemote2w ago
Clinical TrialsComplianceEcho
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Responsibilities

  • Serve as an advisor/subject matter expert for cardiovascular imaging across the following tasks:
  • Reviewing and developing requests for proposals (RFP) with Business Development and Contracts & Proposals groups
  • Supporting the sales process and increasing sales for the Therapeutic Area
  • Analyzing sponsor protocols to define imaging, read criteria, design and workflow
  • Acting as a liaison with internal and external physician reader groups to establish clear guidelines and appropriate training
  • Providing technical input and support to the Therapeutic Area Operations
  • Developing subject matter expertise in reading software systems and serve as liaison across departments and vendors
  • Participating in development of study procedure manuals, imaging charters, training documents, end of study reports and applicable standard operating procedures (SOPs)
  • Establishing partnerships with client imaging groups
  • Drafting capabilities presentations and participating in client bid defenses
  • Assisting in the creation and development of applicable research papers and editorials
  • Identifying innovations for central read efficiencies and interpretation techniques
  • Interpreting and developing operational strategies for new imaging criteria and applicable training
  • Assisting in the execution of specialized client project requests including study case image presentations
  • Participating in user acceptance testing for new tools and software enhancements
  • Exploring new opportunities to add value to organization and departmental processes
  • Communicating with different internal departments regarding image quality, deliverables, data discrepancies, and issues needing resolution
  • Attending project specific, system, and team focused training
  • Training employees in imaging modalities and system applications, including proprietary and 3rd party Software.
  • Attending and participating in applicable company-sponsored training and/or industry conferences
  • What We Look For
  • College degree in science or health-related field, or equivalent experience.
  • Modality related training required (Cardiovascular Imaging- Echo, CMR, and/ or CCTA)
  • Minimum 5 years of experience in clinical research or imaging related field
  • Understanding of therapeutic area-specific imaging acquisition and reconstruction principles
  • Understanding of therapeutic area-specific imaging analysis and measurement methods
  • Understanding of Good Clinical Practice
  • Multilingual capabilities a plus
  • Strong professional communication skills (English), including reading, writing and verbal communication.
  • Ability to work virtually, in group setting and independently
  • Excellent attention and orientation toward meticulous work
  • Strong motivational skills and abilities, promoting a team-based approach
  • Strong interpersonal and communication skills, both verbal and written
  • Strong organizational skills
  • Goal-oriented and ability to adjust to changing priorities
  • Ability to project and maintain professional and positive attitude
  • Strong computer skills

Benefits

Competitive compensationComprehensive health, dental, and vision coverageRetirement savings plan with company contributionPaid time off and company holidaysHealth insuranceDental insuranceVision insurance

Additional Information

At Clario, part of Thermo Fisher Scientific, we develop regulated technology that helps unlock better evidence and improve patient outcomes worldwide. Our software platforms support clinical trials, diagnostics, and medical decision-making in highly controlled regulatory environments. As a Research Technologist within Cardiovascular Imaging in Medical & Scientific Affairs, you will support the development, review, and delivery of scientific content and research outputs for trails with cardiovascular imaging components in a regulated clinical environment. This role involves collaborating with cross-functional teams to ensure accuracy, quality, and compliance of medical and scientific materials, while contributing to evidence generation and supporting clinical and regulatory initiatives.


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