Imaging Research Associate I at Clairo

Budapest, Hungary

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Not SpecifiedCompensation

Entry Level & New GradExperience Level

Full TimeJob Type

UnknownVisa

Clinical Trials, Medical Imaging, HealthcareIndustries

Requirements

High school diploma required; Associate/Bachelor’s degree in bioscience, computer science, IT or related field preferred
Familiarity with PC-based systems and standard software (Word, Excel, databases)
Understanding of clinical trials and good clinical practices preferred
Experience navigating networks and managing files
Ability to work independently and in teams; adaptable to changing priorities
Excellent attention to detail and strong documentation skills
Effective verbal and written communication skills
Professional and positive attitude
Based in or able to work from Budapest (hybrid)

Responsibilities

Prepare and reproduce study materials during start-up
Follow up on site documentation and schedule training sessions
Create test run requests and review incoming study data
Monitor and resolve data discrepancies and manage site communications
Generate and verify reports for sites and sponsors
Investigate logistical edit checks and report system issues
Coordinate and process IQC data including phantom rotation and machine equivalence
Maintain IQC tracking databases and ensure protocol compliance
Track IQC submissions and communicate progress to study teams
Maintain study databases and prepare BMD Scan Review Forms
Plan and coordinate site start-up activities and training
Enter and track data in internal systems and participate in project meetings
Review project tracking, resolve queries, and identify site/data trends
Manage site communications and assist with client issue resolution
Respond to inquiries professionally and maintain SOP compliance
Participate in SOP updates and company-sponsored training

Skills

Excel

Word

databases

clinical trials

data management

site coordination

training sessions

data review

query resolution

SOP compliance

PC systems

file management

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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