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 Clinical Programmer Analyst

Details
Country: USA
Location: New Jersey-Northern Mahwah
Total applied: 7
Job Category:Biotech/R&D/Science
Location:US-NJ-Mahwah
Status:Full Time
Occupations:Clinical Research
Career Level:Experienced (Non-Manager)
Clinical Programmer Analyst

Stryker is an exceptional company with exceptional people who deliver exceptional results. We have differentiated ourselves by responding in innovative ways to the needs of our global customers and patients. We have created a work environment that attracts talented, driven people who love to win and to serve others. We hold ourselves accountable to reach or exceed our goals and to continually improve everything we do. These attributes are shared by the employees that make up Stryker. They are the things that bring us together. They are the foundation of all we do. And they are the enablers of both our past and future success.Stryker is one of the world’s leading medical technology companies with the most broadly-based range of products in orthopaedics and a significant presence in other medical specialties. Stryker works with respected medical professionals to help people lead more active and more satisfying lives. The Company's products include implants used in joint replacement, trauma, craniomaxillofacial and spinal surgeries; biologics; surgical, neurologic, ear, nose & throat and interventional pain equipment; endoscopic, surgical navigation, communications and digital imaging systems; as well as patient handling and emergency medical equipment. The Company's website address is http://www.stryker.com

Provide technical programming and analytical support to Clinical Data Management Systems (CDMS) in the day-to-day operation. Develop and support new clinical studies. Participate in validation and UAT processes.
Create and maintain data entry screens with Adobe Designer; incorporate business rules via JavaScript; integrate new forms into NetRegulus application.Participate in migration activities; includes providing aid in writing insertion views and validating output data.Participate in clinical studies meetings and CRF standardization efforts.Assist System Administrator with implementation of new forms, variable and reporting table standardization.Participate in validation, including testing and documentation (e.g., requirements document, IQ/OQ and UAT scripts, change controls), in accordance with GCP and company standards.Troubleshoot current applications and resolve coding issues.Write SQL to create data edit checks.Develop and maintain Crystal reports to support efficient data retrieval and review. Interact with SAS programmers to provide data reporting and cleaning support.Interact effectively with Data Management and Study Management teams to achieve department objectives.1-2 years of SQL or PL/SQL experience.2 years of experience with SQL Server 2000 tools.1- 2 year of experience with VB6 or/and .NETKnowledge of Adobe LiveCycle (Adobe Designer 7.0) or other Adobe form development software highly preferred.Must have working experience with JavaScript.Crystal reports 8.5 and up is a plusExperience in code development, error handling and troubleshooting a must.Experience analyzing database schemas to quickly grasp domain concepts and how data is stored.Highly customer service oriented and excellent communication skillsExperience working independently and as a team memberBachelor s Degree in Information Systems or other relevant field of study.Stryker is an equal employment opportunity/affirmative action employer committed to hiring a diverse workforce.To read more about Stryker, please visit our website at www.stryker.com

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