Clairo

Imaging Research Associate I

Costa Rica

Not SpecifiedCompensation
Entry Level & New GradExperience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Clinical Research, Medical DevicesIndustries

Requirements

Candidates should possess a Bachelor’s degree in a related scientific field, such as Biology, Chemistry, or a related discipline, and have at least one to two years of experience in imaging research, clinical trials, or a related field. Strong organizational and communication skills are essential, along with the ability to work independently and as part of a team. Familiarity with clinical trial processes and data management systems is preferred.

Responsibilities

The Imaging Research Associate I will coordinate all site and operational activities throughout a clinical trial, ensuring timely delivery of high-quality service deliverables. They will assist in preparing study materials, follow up on outstanding documentation from clinical sites, schedule logistical and technical trainings, create test run requests, review and process study data, manage site communications, investigate data discrepancies, and perform day-to-day IQC activities including data review, coordination of cross calibration phantom rotation, and machine equivalence analysis. Additionally, they will support project administration by planning site start-up activities, maintaining study databases, participating in project meetings, and ensuring client satisfaction.

Skills

Clinical trial coordination
Data management
Study start-up procedures
Document reproduction and tracking
Logistical planning
Data discrepancy resolution
System issue reporting
IQC activities
Phantom data analysis
Cross calibration

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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