The Role
Lead the programming and administration of clinical databases using Medidata Rave, ensuring compliance with standards, and providing technical support for study development.
Summary Generated by Built In
Work Flexibility: Hybrid
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
Skills 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 and database build
- Medidata Rave 5.6.4 Certified Study Builder
- C# programming
- Hands-on experience with clinical studies, including EDC design and CRF development
Inari Medical Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.
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Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
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Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
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Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.
Inari Medical Insights
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The Company
What We Do
Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.
