Clinical Data Processor , Specialty Solutions at Clairo

Bengaluru, Karnataka, India

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Not SpecifiedCompensation

Entry Level & New GradExperience Level

Full TimeJob Type

UnknownVisa

Healthcare, Clinical TrialsIndustries

Requirements

High school diploma or Associate/Bachelor’s degree in computer science, information technology, or related field
0–2 years of experience in clinical trials, healthcare, or a related domain; 1+ year preferred
Proven expertise in MS Office tools including Word, Excel, Teams, and OneNote
Strong proficiency in identifying PII/PHI and applying Good Documentation Practices
Demonstrated ability to work independently and collaboratively in dynamic environments
Fluency in English (written and verbal)

Responsibilities

Execute study-specific workflows including creation, resumption, cancellation, and completion of Workflow Runs
Review and redact images, videos, and documents per study parameters and timelines
Provision customer user accounts for assigned studies and trials
Facilitate source document translation and create DICOM image links as needed
Use tools such as SightHound and PDF redaction software to process source documents
Issue queries and follow up with study sites to resolve documentation issues
Support generation and distribution of final study closeout deliverables
Collaborate with cross-functional teams to ensure proper tool usage and adherence to specifications
Attend project and team meetings to align on study progress and expectations
Maintain high standards of quality, professionalism, and accountability in all deliverables

Skills

MS Office

Excel

Word

Teams

OneNote

PDF redaction

SightHound

PII identification

PHI identification

Good Documentation Practices

DICOM

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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