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Clario Hiring for Clinical Data Management Associate

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B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Computer Science, Healthcare, Clinical Research, Data Science, or a related field, or equivalent professional experience

India – Remote

3+ years

Verified Job

Online Application

Clario, a part of Thermo Fisher Scientific, is hiring for the position of Clinical Data Management Associate II in India. This is a full-time remote opportunity for candidates with experience in Clinical Data Management, clinical research, biotechnology, pharmaceutical, or related healthcare environments.

The selected candidate will support clinical trial data management activities, including data validation, edit checks, data quality review, study documentation, and issue resolution for medical imaging studies.

Clario Recruitment 2026 – Job Details

ParticularsDetails
CompanyClario
Parent OrganizationThermo Fisher Scientific
Job RoleClinical Data Management Associate II
Job LocationIndia – Remote
Job TypeFull-time
ExperienceMinimum 3+ years
Job Requisition IDR18060
Job Posting06 November 2026
Work ModeRemote
Application ModeOnline

Position Available

Clinical Data Management Associate II

The Clinical Data Management Associate II will work within Clario’s Medical Imaging business, supporting the review, validation, and management of clinical trial data generated from imaging studies across multiple therapeutic areas.

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The role involves collaborating with project teams, sponsors, and operational stakeholders to maintain clinical data accuracy, support study execution, and ensure reliable clinical research data.

Key Responsibilities

  • Review study documentation and project requirements to assess their impact on clinical data management processes and deliverables.
  • Support study setup, data collection strategies, and implementation of data management plans.
  • Define, execute, review, and maintain edit checks to identify data discrepancies.
  • Review clinical and imaging-related data to identify inconsistencies and quality issues.
  • Develop and maintain data specifications, including data transfer and system configuration specifications.
  • Create, review, and maintain transmittal forms and study documentation.
  • Investigate and resolve clinical data discrepancies in collaboration with project teams.
  • Track data-related issues and ensure timely resolution.
  • Prepare, validate, and deliver data listings and study reports.
  • Identify system enhancements, bugs, and process improvement opportunities.
  • Maintain accurate and audit-ready study documentation throughout the study lifecycle.
  • Communicate project status, risks, and data quality concerns to stakeholders.
  • Contribute to SOP updates and departmental quality improvement initiatives.
  • Ensure compliance with company procedures, Good Clinical Practice (GCP), and applicable regulatory expectations.

Eligibility and Qualifications

Candidates interested in the Clinical Data Management Associate II position should meet the following requirements:

  • Bachelor’s degree in Computer Science, Life Sciences, Healthcare, Clinical Research, Data Science, or a related field, or equivalent professional experience.
  • Minimum 3+ years of experience in Clinical Data Management, clinical research, biotechnology, pharmaceutical, CRO, or related healthcare environments.
  • Understanding of clinical trial processes and clinical database management principles.
  • Working knowledge of relational database concepts, data validation techniques, and quality control processes.
  • Experience developing or maintaining data specifications, edit checks, data transfer requirements, or study configuration documentation is preferred.
  • Familiarity with clinical trial terminology and regulated research environments.

Required Skills

  • Clinical Data Management and clinical data review.
  • Clinical database management principles.
  • Data validation and quality control.
  • Edit checks and data discrepancy resolution.
  • Relational database concepts.
  • Microsoft Office: Word, Excel, Access, Outlook, and PowerPoint.
  • Analytical and problem-solving skills.
  • Strong attention to detail and data accuracy.
  • Documentation and time-management skills.
  • Excellent written and verbal English communication.
  • Ability to work independently and collaborate with global cross-functional teams.

Salary and Benefits

Clario offers the following benefits for this position:

  • Competitive pay and incentives.
  • Provident fund.
  • Medical insurance.
  • Employee engagement programmes and local events.
  • Modern office spaces and remote work flexibility.
  • Professional growth and career development opportunities within a global organization.
APPLICATION DETAILS

How to apply

Apply online

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