Stryker · 1 day ago
Principal Clinical Data Systems Specialist (Remote)
United States
Full-time
Remote
Lead/Staff
$126K/yr - $274K/yr
8+ years expStryker is seeking a Principal Clinical Data Systems Specialist to join our Neurovascular division. This role involves providing data management expertise and support to Core teams, managing Rave URL activities, and leading clinical data and SAS programming activities.
BiotechnologyHealth CareLife ScienceMedicalMedical Device
Responsibilities
Manage administration of the Rave URL activities: Report Administration, eLearning, User Roles and Core Configuration
Provide technical support for Rave study development, Rave URL modules, and site management/user access within Medidata Client Division
Lead development of study database development, including but not limited to, programming of clinical database according to CRF Specifications and programming of edit checks (edit checks, derivations, and custom functions) according to Edit Check Specifications
Support Stryker Neurovascular Global Library by programming forms, edit checks (edit checks, derivations, and custom functions) according to Stryker NV data collection standards
Lead Clinical Data and SAS Programming activities
Create and maintain Clean Patient Trackers, dashboards and operational reports
May serve as system administrator to grant user and site access using Medidata Cloud Administration for Rave (EDC and Modules), Coder, RTSM and MMI (Imaging)
Follow Stryker standard processes and maintain proper documentation in performance of Medidata product administration and development activities within the Medidata Client Division and Rave URL
Qualification
Required
Bachelor's degree
8+ years of clinical data management experience in medical device or pharma
Proven expertise as a Medidata Rave super user, including URL management, database build, configuration, testing, and validation for global clinical trials
Hands-on experience with PMV clinical studies, including EDC design, CRF development, edit checks, and UAT
Strong knowledge of data collection, reconciliation, processing, coding, reporting, and validation across clinical trial data workflows
Deep understanding of clinical data management systems and regulatory standards (ICH GCP, ISO14155, Good Data Management Practices, IDE, HIPAA, GDPR, 21 CFR Part 11)
Preferred
Master's Degree in a technical or scientific discipline
Medidata Rave 5.6.4 Certified Study Administrator, Medidata Rave 5.6.4 Certified Study Builder
Working knowledge of SAS programming, electronic data capture, and XML
C# programming
Medidata Imaging Platform
Previous experience with complex, global trials
Benefits
Medical and prescription drug insurance
Dental insurance
Vision insurance
Critical illness insurance
Accident insurance
Hospital indemnity insurance
Personalized healthcare support
Wellbeing program
Tobacco cessation program
Health Savings Account (HSA)
Flexible Spending Accounts (FSAs)
401(k) plan
Employee Stock Purchase Plan (ESPP)
Basic life and AD&D insurance
Short-term disability insurance
Company
Stryker
Stryker is a medical technology company that offers products and services in orthopaedics.
10001+ employees
H1B Sponsorship
Stryker has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (105)
2024 (76)
2023 (63)
2022 (78)
2021 (57)
2020 (77)
Funding
Current Stage
Public CompanyTotal Funding
unknown1990-01-02IPO
Leadership Team
Kevin Lobo
Chair & CEO
Glenn S. Boehnlein
Chief Financial Officer and Vice President
Recent News
GlobeNewswire News Room
2025-02-11
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