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Clinical Programmer Analyst II Princeton United States,  


Posted on : 02 May 2017

Project Description

Tracking Code 1612-050 Job Description Bioclinica, Inc. is looking for intelligent, creative and dedicated professionals to join our growing team. We are a company that values technical excellence, teamwork and a commitment to success. We employ cutting edge technology to provide our customers with industry leading solutions and are currently seeking to fill the position of Clinical Programmer Analyst II to work out of our Princeton, NJ/remote office. Primary Responsibilities Provides data to clients (internal and external) in functional format by: Creating and executing SAS edit check programs Validating edit check programs using standard validation practices and processes Creating, validating and executing SAS programs and macros Utilizing SAS programming skills to provide ad-hoc reports (external and internal) Assist in developing programming specifications Assist in creating program specific validation plans Identify and implement solutions for complex reporting needs Ensures client data accuracy and integrity by: Creating and/or reviewing data editing and export specifications Works directly with clinical data manager, and where needed with clinical project manager and other team members to ensure specifications are clear and accurate. Has a clear understanding of the contextual requirements for reporting outputs; and provides feedback Programming data cleaning/consistency checking programs to support internal applications for all therapeutic areas Programming and testing data export programs in accordance with specific client needs Documenting all programming and validation efforts in accordance with Good Clinical Practices Monitoring data integrity throughout a given study Utilizing SDTM guidelines to create transfer datasets Participating in project meetings (internal and external) Develops and maintains clinical programming standard operating procedures by: Participating in the development of data editing conventions, specification documents and Clinical Data Management (CDM) processes Contributing to, design and maintain a library of reusable code Leading and managing enhancements to current CDM systems and providing inputs in the implementation of new systems. Ensures project timelines are maintained by: Working independently and efficiently with minimal input required from the manager. Reviewing timelines; and projecting estimates and target dates in conjunction with direct supervisor and project team Adhering to target dates for project timelines Communicating any changes in target date to appropriate personnel including Project Manager Keeping department head informed of progress as well as potential impediments Maintains Quality Service and Departmental Standards by: Adhering to established processes and standards Reading, understanding and adhering to organizational Standard Operating Procedures (SOP Assisting in establishing and enforcing departmental standards Maintain and review clinical programming SOPs Participating in the modification of company SOPs Job Location Princeton, New Jersey, United States Position Type Full-Time/Regular

Locations

Princeton, New Jersey, United States

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