Data Manager (Permanent role )

United StatesOn-site

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Responsibilities

Manage end-to-end clinical data management activities for assigned studies
Design and review CRFs (Case Report Forms) and edit checks
Oversee data collection, cleaning, and validation processes
Perform data review and discrepancy management
Coordinate with cross-functional teams (Clinical, Biostatistics, Programming)
Ensure compliance with CDISC standards and regulatory guidelines
Support database build, UAT testing, and database lock activities
Generate and review data listings and reports
Ensure timely delivery of high-quality datasets for analysis and submission Required

experience in a CRO or pharmaceutical environment. The role involves managing clinical trial data to ensure accuracy, integrity, and compliance with regulatory standards. Key Responsibilities:
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field 3–5 years of
experience in clinical data management within CRO/pharma Hands-on
experience with EDC systems (e.g., Medidata Rave, Oracle Clinical, Inform)
Strong understanding of GCP, ICH guidelines , and clinical trial processes
Familiarity with CDISC standards (SDTM)
Good knowledge of data validation and query management
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...
ClinChoice is currently recruiting for a Clinical Data Manager to join our team in a permanent position—an exciting opportunity to lead impactful statistical strategy in a dynamic environment. Role Overview:
Participate in data reconciliation (e.g., SAE, lab data)