Automation Analyst at Clairo

Bengaluru, Karnataka, India

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

N/AIndustries

Requirements

Bachelor’s Degree in Computer Science, Engineering, Life Sciences or related field required; Master’s preferred
4+ years’ experience in validation/software testing required
Experience working with test automation tools – such as Coded UI, Selenium, Ranorex, Test Complete preferred
Experience working with computer software including Word, Excel and Access preferred
2+ years’ experience working with clinical trials and/or within pharmaceutical environment preferred
Working knowledge of the drug development process including knowledge of FDA requirements for GxPs and 21 CFR Part 11 preferred
Proven problem-solving abilities
Ability to adjust to changing priorities
Strong understanding of automated software QA methodologies
Excellent attention to detail and orientation toward careful meticulous work
Must be highly motivated, result-oriented, and possess the ability to handle multiple projects with multiple deadlines concurrently with minimal supervision
Strong problem-solving, documentation and organizational skills
Excellent oral and written communication skills
Ability to project and maintain a professional and positive attitude

Responsibilities

Ensures software applications are accurate, complete and conform to all user, company and regulatory requirements by planning, creating, and implementing automated verification processes
Creating associated validation documentation using proper documentation methods
Assisting in the development and maintenance of automated testing procedures, processes, and quality standards
Performing troubleshooting methods as necessary to maintain a stable and effective automated testing environment
Working with software developers to resolve issues and retest applications
Evaluating and analyzing test results
Participating in project team meetings as needed
Updating automated test scripts by maintaining scripts and associated test matrices
Identifying new areas for regression testing
Mentors junior validation staff by assisting in the quality review of automated validation packages and providing related feedback
Assisting staff with problem solving and troubleshooting issues
Maintains Quality Service and Departmental Standards by reading, understanding and adhering to organizational Standard Operating Procedures (SOPs)
Assisting in establishing and enforcing departmental standards including defining, documenting and implementing validation standards as needed
Contributes to team effort by training staff on departmental processes, validation protocol, testing techniques and documentation methods
Performing code reviews and offering feedback on best coding practices when necessary
Evaluating, monitoring and prioritizing workload of staff to ensure projects are on time; affecting change when necessary
Offering technical and quality feedback/advice to both internal and external clients
Working with internal staff including technical staff, project managers and applications developers to assist with the development of project specifications
Exploring new opportunities to add value to organization and departmental processes
Helping others to achieve results
Performing other duties as assigned
Maintains Technical and Industry Knowledge by attending and participating in applicable company-sponsored training

Skills

Automated Testing

Test Automation

Validation Documentation

Regression Testing

Test Scripting

Troubleshooting

Code Review

Quality Assurance

SOP Compliance

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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