Clinical Data Manager

Clario

Bengaluru

On-site

INR 800,000 - 1,200,000

Full time

14 days+

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Benefits offered by this job

Competitive pay
Provident fund
Medical insurance
Remote work flexibility

Job summary

Clario, part of Thermo Fisher Scientific, is seeking a Data Management Specialist to lead data management deliverables for clinical studies. You will attend client meetings, implement study requirements, and develop edit checks with project teams to ensure data integrity.

The role requires a Life Sciences degree and 3+ years in clinical data management, with knowledge of relational databases and SAS desirability. Hybrid/remote options available, based in India.

Qualifications

  • Bachelor’s degree in Life Sciences, or related field.
  • 3+ years of clinical data management experience in pharma/biotech/CRO.
  • Relational databases and validation knowledge.
  • Familiarity with SAS preferred; strong data management skills.

Responsibilities

  • Perform all data management deliverables for assigned studies.
  • Attend and participate in client meetings as requested.
  • Understand requirements for study implementation and data collection.
  • Collaborate with project teams to develop study-specific edit check criteria.
  • Define, run, and review edit checks; resolve discrepant data.
  • Maintain organized, complete, and up-to-date study documentation.
  • Perform study setup including TF design, database structure, and specifications.
  • Coordinate and document receipt and processing of data from external sources.
  • Review data for errors and inconsistencies; collaborate to resolve issues.
  • Track outstanding issues and follow up until resolution.
  • Ensure CDM activities comply with regulatory guidelines.
  • Adhere to SOPs and departmental standards; assist in SOP updates.
  • Contribute to team efforts and explore opportunities to add value.

Skills

Attention to detail
Interpersonal communication
Problem solving
Independent yet collaborative

Education

Bachelor’s degree in Life Sciences

Tools

SAS
Microsoft Word
Microsoft Excel
Microsoft Access

Job description

At Clario, part of Thermo Fisher Scientific. Join us as a global leader in clinical trial endpoint technology and help transform evidence generation for better patient outcomes.

What We Offer
  • Competitive pay and incentives
  • Provident fund and medical insurance
  • Engaging employee programs and local events
  • Modern office spaces and remote work flexibility
What You’ll Be Doing
  • Perform all data management deliverables for assigned studies
  • Attend and participate in client meetings as requested
  • Understand requirements for study implementation and data collection
  • Collaborate with project teams to develop study-specific edit check criteria
  • Define, run, and review edit checks; resolve discrepant data
  • Maintain organized, complete, and up-to-date study documentation
  • Perform study setup including TF design, database structure, and specifications
  • Coordinate and document receipt and processing of electronic or ancillary data from external sources
  • Review data for errors and inconsistencies; collaborate to resolve issues
  • Track outstanding issues and follow up until resolution
  • Ensure CDM activities comply with regulatory guidelines
  • Adhere to SOPs and departmental standards; assist in SOP updates
  • Contribute to team efforts and explore opportunities to add value
  • Maintain technical and industry knowledge through training
What We Look For
  • Bachelor’s degree in Life Sciences, or related field (or equivalent experience)
  • 3+ years of experience in clinical data management within pharma, biotech, or CRO industry
  • Working knowledge of relational database organization and validation
  • Familiarity with SAS desirable
  • Proficiency with Word, Excel, and Access preferred
  • Understanding of clinical trial terminology desirable
  • Strong problem-solving skills and attention to detail
  • Ability to work independently and in a team setting; adaptable to changing priorities
  • Excellent interpersonal and communication skills
  • Strong documentation and organizational abilities
  • Based in or able to work from India (remote/hybrid options available)
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