Clairo

Clinical Data Programmer

Costa Rica

Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Biotechnology, Clinical Trials, HealthcareIndustries

Requirements

Candidates should possess a Bachelor’s or Master’s degree in computer science, life sciences, or a related field, with 1-3 years of programming experience in the pharmaceutical industry, and experience working with CDISC, SQL, and relational databases is preferred. A solid understanding of database organization and data extraction techniques is also required, along with demonstrated programming skills and an understanding of medical data.

Responsibilities

The Clinical Data Programmer will provide data to clients in functional format by creating and executing edit check programs, validating these programs, and utilizing programming skills to develop ad-hoc reports. They will assist in developing programming specifications, create program-specific validation plans, identify and implement solutions for complex reporting needs, ensure client data accuracy and integrity by creating data editing specifications, and work directly with clinical data managers to ensure specifications are clear and accurate. Additionally, they will monitor data integrity throughout studies, utilize SDTM guidelines to create transfer datasets, participate in project meetings, develop and maintain clinical programming SOPs, contribute to the development of data editing conventions, and ensure project timelines are maintained by working independently and efficiently. The role also involves documenting programming and validation efforts, maintaining technical and industry knowledge through training, and contributing to team efforts by resolving issues and exploring new opportunities to add value to the organization.

Skills

SAS
Programming
Validation
Data Management
Clinical Data Standards
SDTM
Data Export
Data Cleaning
Reporting
Validation Plans
Ad-hoc Reporting
Data Integrity

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.

Key Metrics

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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