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Senior Staff Clinical Data Systems Specialist

Stryker -
Bengaluru, Karnataka

Apply Now

Job details

Full-time

Benefits

Health insurance

Qualifications

SAS
C#
.NET
Bachelor's degree
Clinical trials
Data collection

Full job description

Why join Stryker?

Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

Job description

We are excited to be named one of the World’s Best Workplaces by Fortune Magazine!
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.

What will you do

Lead Clinical Database Programming activities.
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.
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.

What you need

Required

Bachelor’s Degree in technical or scientific discipline
8+ years of clinical database programming experience in CRO, medical device, or pharma
Proven expertise as a Medidata Rave super user, including URL management, database build, amendment manager, quick publish, core configuration, testing, and validation for global clinical trials
Medidata Rave 5.6.4 Certified Study Builder
C# programming
Global Library Development
Hands-on experience with 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

Preferred

Medidata: eCOA, TSDV, Rave Web Services (RWS)
Zelta EDC2 Certified Basic Designer
Base SAS
Previous experience with complex, global trials

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.

Apply Now

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