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Clinical Validation Analyst

ICR Sweden - SWE · icon.com
ChennaiOn-siteMid level2+ yrs
Apply on ICR Sweden - SWE’s site

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The job in short

Clinical trial data validation and edit check testing.

RecruitmentClinicalSQL

Details

Found
26 d ago · posted 2026-09-08
Location as listed
India, Chennai; India, Bangalore
Role
Lab / Clinical Research
Source
The company’s own careers site

Full description

Clinical Validation Analyst, Chennai/Bangalore/Trivandrum, Office based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Clinical Validation Analyst at ICON, you will ensure the accuracy and integrity of clinical trial data through rigorous validation processes. What You Will Do: You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: • Conducting data validation and quality assurance checks to ensure the integrity of clinical trial data. • Collaborating with cross-functional teams to define validation requirements and develop validation plans. • Identifying and resolving data discrepancies, documenting findings, and recommending corrective actions. • Supporting the development and maintenance of validation documentation, including protocols and reports. • Staying updated on industry best practices and regulatory requirements related to data validation. Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience: • Degree in life sciences, statistics, computer science, or a related field. • Minimum 2 years of experience in Edit Check Testing, Clinical Validation of backend listings. • Experience in clinical data management, validation, or a related role within a clinical research environment. • Strong analytical skills and attention to detail in data analysis and validation processes. • Familiarity with statistical software and data management tools. • Effective communication skills, with the ability to collaborate with diverse teams and stakeholders. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: • Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply

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