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ClarioCL

Research Technologist, Medical & Scientific Affairs

Clario is a leading healthcare research and technology company that enhances clinical trial management through comprehensive endpoint solutions and scientific expertise.

Clario

Employee count: 1001-5000

Costa Rica only

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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.

What We Offer

  • Competitive compensation
  • Comprehensive health, dental, and vision coverage
  • Retirement savings plan with company contribution
  • Paid time off and company holidays

What You’ll Be Doing

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

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

About the job

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Posted on

Job type

Full Time

Experience level

Education

Bachelor degree

Experience

5 years minimum

Experience accepted in place of education

Location requirements

Hiring timezones

Costa Rica +/- 0 hours

About Clario

Learn more about Clario and their company culture.

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At Clario, we understand that our customers face challenges in conducting clinical trials that yield reliable evidence while ensuring safety, efficacy, and quality of life for patients. This is why we leverage our 50+ years of clinical trial data management expertise to drive innovation and deliver dependable solutions. Our primary aim is to empower pharmaceutical, biotech, and medical device companies to transform lives by providing the richest clinical evidence available.

We specialize in endpoint technologies and comprehensive management services for clinical trials, supporting over 26,000 studies in more than 100 countries. Our solutions integrate deep scientific expertise with advanced technology, ensuring accurate data collection and analysis. With our unmatched operational scale and global reach, we facilitate seamless trial execution, enhance patient engagement, and ensure adherence to regulatory standards. At the heart of our mission is a commitment to not only improve data reliability but also elevate the patient experience, making their health and well-being our top priority.

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