Senior Clinical Data Manager — Remote, End-to-End CDM

Princeps Technologiees

United States

Remote

USD 120,000 - 180,000

Full time

4 days ago
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Job summary

Zoho is seeking a Senior Clinical Data Manager to own data management across the full clinical trial lifecycle, from study start-up through close-out. This fully remote role is open to USA/Canada-based candidates, requiring hands-on CDM experience and strong regulatory awareness.

The role includes designing the DMP, CRF specs, eCRF/EDC testing, data validation, and ongoing data quality checks, while coordinating with CROs, programming, statistics, and safety to keep studies on schedule and

Qualifications

  • Bachelor’s degree in Life Sciences, Health Sciences, Pharmacy, Nursing, Computer Science, or a related field.
  • 8+ years of hands-on clinical data management experience in pharma/biotech/CRO.
  • Strong working knowledge of at least one major EDC system (Medidata Rave, Oracle InForm/Clinical One, Veeva CDMS).
  • Familiarity with CDISC standards (CDASH, SDTM) and MedDRA/WHO Drug dictionaries.

Responsibilities

  • Develop the Data Management Plan (DMP) and CRF completion guidelines.
  • Design, build, and test eCRFs and EDC databases with validation and UAT.
  • Lead data cleaning, queries, and reconciliation across sites.
  • Oversee CRO/vendor data management activities and ensure inspection readiness.

Skills

Clinical data management
EDC systems
Remote work
Regulatory awareness

Education

Bachelor’s degree in Life Sciences/related field

Tools

Medidata Rave
Oracle InForm/Clinical One
Veeva CDMS

Job description

Zoho is seeking a Senior Clinical Data Manager to own data management across the full clinical trial lifecycle, from study start-up through close-out. This fully remote role is open to USA/Canada-based candidates, requiring hands-on CDM experience and strong regulatory awareness.

The role includes designing the DMP, CRF specs, eCRF/EDC testing, data validation, and ongoing data quality checks, while coordinating with CROs, programming, statistics, and safety to keep studies on schedule and

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