Senior Clinical Data Manager
Company: Cytel
Role summary
Senior Clinical Data Manager is a full-time role at Cytel (remote). Posted 2026-11-03. Experience level: 2-5. No degree required.
- Job title
- Senior Clinical Data Manager
- Company
- Cytel
- Location
- Remote
- Work arrangement
- remote
- Employment type
- full-time
- Category
- Healthcare Support
- Experience level
- 2-5
- Degree required
- No
- Date posted
- 2026-11-03
You’ll love this fully remote opportunity if you have a knack for clinical data accuracy and want to work with a leader in the pharmaceutical research space. It’s a great chance to take ownership of end-to-end data integrity for clinical trials without the barrier of a degree requirement, provided you have the relevant hands-on experience.
Job description
The Senior Clinical Data Manager will provide comprehensive data management support for assigned clinical studies. The SCDM will be responsible for performing ongoing data review to ensure accuracy, completeness, and consistency of clinical trial data in accordance with the study protocol and data management plan. The CDM will have a minimum of four years of clinical data management experience, including hands-on data review experience, and demonstrated proficiency in Medidata Rave.
Responsibilities
Clinical Data Management
Perform ongoing review of clinical trial data to ensure accuracy, completeness, and consistency.
Identify, investigate, and resolve data discrepancies through query management.
Conduct manual and system-driven data reviews in accordance with study protocols and DMPs.
Collaborate with cross-functional teams (Clinical Operations, Biostatistics, Programming, Medical Monitoring) to support data cleaning activities.
Participate in database lock activities and ensure data readiness for interim and final analyses.
Maintain study documentation in compliance with regulatory requirements and internal SOPs.
Manage and maintain user access within clinical data management systems (e.g., Medidata Rave).
Process access requests, modifications, and terminations in accordance with established procedures.
Ensure appropriate role-based access and system permissions are assigned.
Maintain audit-ready documentation related to user access activities.
Support periodic access reviews and compliance checks.
Assist with system user training and troubleshooting as needed.
Qualifications
Bachelor’s degree in Life Sciences, Health Sciences, or a related field (or equivalent experience).
Minimum of 4 years of clinical data management experience.
Demonstrated hands-on data review experience in clinical trials.
Proficiency in Medidata Rave (build knowledge a plus, but not required).
Strong understanding of clinical data management processes and regulatory requirements (GCP, FDA, ICH guidelines).
Experience with query management and discrepancy resolution.
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