Clinical Data Manager
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 36d ago
The date the source published, not the day we noticed it (2026-08-26). Last seen at its source just now.
We have tracked this listing since 22 Sep 2026 (8 days). The employer's own board has carried it every time we have read it, most recently just now.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
India
The description states no restriction of its own. This is the source's own tag.
Carried by 1 source
-
workday employer's own board first seen 8d ago · last seen just now
- location not stated
The listing
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.