Clinical Research Data Associate Manager
Key Skills for This Role
Full Job Posting
What you will do
- Lead clinical data management activities across the study lifecycle, including database planning, data review, query management, database freeze/lock readiness, study reporting, and study closeout activities.
- Design, build, and maintain clinical databases, CRFs/eCRFs, workflows, edit checks, and data collection processes aligned with protocol requirements and study objectives.
- Develop and execute data management plans, review strategies, timelines, and documentation to ensure data integrity, quality, compliance, and inspection readiness.
- Establish and monitor key study milestones, including database go-live, interim analyses, database freezes, database lock, data transfers, and archival activities.
- Lead data cleaning, review, and issue resolution activities by identifying trends, managing queries, investigating discrepancies, and implementing corrective actions to ensure accurate and reliable study data.
- Collaborate with cross-functional stakeholders, including Clinical Operations, Clinical Insights, Safety, Biostatistics, Programming, and Regulatory Affairs, to support study execution, reporting, regulatory submissions, and data-driven decision making.
- Support database validation, user acceptance testing (UAT), change control activities, and continuous improvement initiatives to enhance data management processes, standards, and system performance.
- Generate data reports, metrics, dashboards, and study summaries; provide training, guidance, and oversight to study personnel and data management team members to promote consistent data quality practices.
Required Qualifications
- Bachelor’s degree
- Minimum of 6+ years of clinical data management experience supporting clinical trials in the medical device, medical technology, or pharmaceutical industry.
- Experience leading or contributing to departmental initiatives, strategic planning efforts, or organizational improvement projects.
- Demonstrated experience independently leading data management activities across multiple complex clinical studies.
Preferred Qualifications
- Experience leading end-to-end clinical data management activities across multiple studies and throughout the study lifecycle.
- Advanced experience with CRF/eCRF design, clinical database development, edit check specification, validation, and UAT.
- Proficiency with SQL and/or other data review and reporting tools used to identify trends, data quality issues, and opportunities for process improvement.
- Posted Date: 10/01/2026 This role will be posted for a minimum of 3 days.
United States of America Pay Ranges
- USN : $110,100 - $183,400 USD Annual
- US5 : $115,600 - $192,600 USD Annual
- US10 : $121,100 - $201,700 USD Annual
- US15 : $126,600 - $210,900 USD Annual
- US20 : $132,100 - $220,100 USD Annual
- US30 : $143,100 - $238,400 USD Annual
About Stryker
Global leader in medical technologies for orthopaedics, medical, surgical, and neurotechnology.
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