Clario
Clinical Data Manager
India · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerClario
- LocationIndia
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
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. As a Clinical Data Manager, you will review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across diverse therapeutic areas, ensuring accuracy, compliance, and quality throughout the data lifecycle.
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
Show full description
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)
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
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Skills in this posting
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