Validation Analyst at Clairo

Bengaluru, Karnataka, India

Clairo Logo
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Information TechnologyIndustries

Requirements

Candidates should possess a Bachelor's degree in computer sciences or equivalent relevant work experience in a software testing environment, with approximately 4 to 6 years of experience in software quality testing. Experience with pharmaceutical-related software is preferred. A deep understanding of software quality assurance, ideally in a Clinical Data environment, is required. Proficiency in writing SQL queries for data validation and identifying quality issues is essential, along with experience in project delivery methodologies such as SDLC, Iterative, Agile, Scrum, and Kanban. Knowledge of SDLC testing methodology and document management, along with proficiency in Microsoft Office Suite tools, is necessary. Experience in writing test cases based on product requirements and collaborating with development and business teams is also required. Preferred qualifications include creativity and initiative to enhance product test coverage and effectiveness, experience with web-based SAAS platforms, and knowledge of cloud-based testing.

Responsibilities

The Validation Analyst will be accountable for high-quality and on-time delivery of assigned tasks, tracking software versions, features, bugs, and validation efforts, and developing/utilizing test data sets. They will create and execute manual test scripts to ensure software quality and functionality using defined validation protocols and techniques, and generate associated validation documentation. Responsibilities include working with application developers to resolve issues and retest applications, and participating in the testing of new Clario products by developing test cases, conducting general and Clinical Services development tool testing, and reporting anomalies. They will also participate in post-production product release testing by developing test cases, performing regression and bug fix testing for Clinical Services, and reporting anomalies. Secondary responsibilities include exploring opportunities to add value to organizational and departmental processes, attending training, adhering to SOPs, establishing and enforcing departmental standards, assisting colleagues, and performing other assigned duties. This includes keeping informed of regulatory changes and benchmarking state-of-the-art practices.

Skills

SQL
PL-SQL
PySpark
Python
SAS
Tableau
Power BI
Data Lakes
Data Warehouse
ETL
SDLC
Agile
Scrum
Kanban
JIRA
Azure DevOps
Confluence
Data Quality
Data Governance
Smoke Testing
Integration Testing
System Testing
Regression Testing
Test Data
Manual Testing
Documentation
MS Office

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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