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Clarioclinical

Clinical Data Manager

Bangalore, India · India Remote

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hirly's read of this role

Seniority
Lead / management
Country
IN
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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

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.

Original posting on Clarioclinical's site ↗

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