Clairo

Ophthalmic Medical Technologists (f/m/x)

Hungary

Not SpecifiedCompensation
Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Medical Imaging, Clinical ResearchIndustries

Ophthalmic Medical Technologist (f/m/x)

Employment Type: Full time

Location: Budapest, Hungary

Position Overview

Clario is seeking experienced Ophthalmic Medical Technologists with a background in ophthalmology to join our team in Budapest, Hungary.

What We Offer:

  • Competitive compensation
  • Attractive benefits (security, flexibility, support, and well-being)
  • Engaging employee programs
  • Remote working & home office allowance
  • OTP Szép Card

Responsibilities:

Our Ophthalmic Medical Technologists ensure Quality, including Protocol Compliance and Technical Adequacy, of Image Data by:

  • Reviewing and analyzing ophthalmic image data for clarity and quality.
  • Verifying image data is in compliance with project protocol requirements.
  • Generating image queries when needed.
  • Working with therapeutic teams to notify Sponsor/Site for proper resolution of quality issues.
  • Assisting in archiving data for completed projects.

You may also support other image analysis functions by:

  • Performing client or internal demonstrations of image processing.
  • Reviewing and preparing images for submission to client and/or agency.

You’ll help identify and communicate Project Requirements as they relate to the image quality review (IQR) processes by:

  • Reviewing evaluations of potential clinical research sites and verifying the accuracy of information pertaining to site personnel, ophthalmic imaging equipment, imaging protocol, and data archival capabilities.
  • Providing support for technical imaging-related issues.
  • Performing study initiation/technical visits to educate site personnel on image acquisition protocol, data archival, and data transmittal procedures, including form(s) completion.
  • Assisting in the design and implementation of study-related forms.
  • Assisting in writing and reviewing imaging guidelines/manuals.
  • Assisting in reviewing Site Surveys.

Maintain Quality Service and Departmental Standards by:

  • Reading, understanding, and adhering to organizational Standard Operating Procedures (SOPs).
  • Assisting in establishing and enforcing departmental standards.
  • Participating in user acceptance testing for new tools and software enhancements.
  • Participating in the modification of company SOPs related to IQR.

Requirements:

  • Associates/Bachelor’s degree preferred.
  • 2+ years as an Ophthalmic Imaging Technologist or relevant clinical trial experience preferred.
  • Experience with ophthalmic imaging modalities (e.g., OCT, fundus photography) preferred.
  • Experience working with computer software including Word, Excel, and Access preferred.
  • Experience working with clinical trials and/or within a pharmaceutical environment preferred.

Company Information:

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

Skills

Ophthalmic imaging
Image analysis
Protocol compliance
Quality assurance
Data archiving
Image acquisition
Standard Operating Procedures (SOPs)

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters
1972Year Founded
$29.9MTotal Funding
GROWTH_EQUITY_VCCompany Stage
Biotechnology, HealthcareIndustries
5,001-10,000Employees

Benefits

Competitive and equitable total rewards package
Physical, mental and financial health and wellness
Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.
The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.
AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.
The company has nearly 50 years of experience in clinical trial technology solutions.
Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.
The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.
Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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