Clinical Programmer Analyst II

Job Description

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 Identifying and implementing solutions for complex reporting needs Ensures client data accuracy and integrity by:Creating and / or reviewing data editing and export specifications Working 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 , designing and maintaining 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 Secondary Responsibilities Contributes to team effort by:Working with internal staff to resolve issues Exploring new opportunities to add value to organization and departmental processes Helping others to achieve results Performing other duties as assigned Maintains Technical and Industry Knowledge by:Attending and participating in applicable company - sponsored training Qualifications: Education:Bachelor s or Master s degree in computer science , life sciences or related field requiredSAS Certified Professional considered a plusExperience:3 years SAS programming experience in pharmaceutical related industry required (1 year with Master s degree)Experience working with CDISC , SQL , and Relational Databases preferredDemonstrated programming skills requiredWorking knowledge and solid understanding of database organization and how to extract data in order to generate listings and reportsProven ability in analyzing dataUnderstanding of medical and / or clinical trial terminology is desirableProven ability in problem solvingAdditional skill set:Ability to work in group setting and independently; ability to adjust to changing prioritiesExcellent attention to detail and orientation toward meticulous workStrong interpersonal and communication skills , both verbal and writtenStrong documentation and organizational skillsAbility to project and maintain a professional and positive attitudeWorking conditions:Travel: 0 - 5%Lifting: 0 - 10lbsOther: Computer work for long periods of timeEEO StatementBioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race , color , religion , gender , national origin , age , sexual orientation , gender identity or expression , protected veteran status , disability / handicap status or any other legally protected characteristic,

Keyskills :
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