Senior Clinical Programmer
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POST DATE 8/19/2016
END DATE 11/5/2016
JOB DESCRIPTIONPosition Title: Senior Clinical Programmer
Employer: INC Research, LLC.
Job Location: 3201 Beechleaf Court, Suite 600, Raleigh, NC 27604
Hours: Monday Friday, 9:00 am to 5:00 pm
Summary of Duties: Utilizes primary clinical programming development to write, validate, and maintain software to meet specifications following standard development procedures.
Generates and maintains all required documentation, including the development of specifications, coding, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding setup, edit check procedures, import setup and processing, export setup and processing, listings, and profile reporting.
Serves on project teams to coordinate and lead clinical programming activities for projects. Provides technology support to the clinical programming staff.
Provides application administration and technical support as the subject matter expert on core business packages and supplemental packages.
Ensures high quality deliverables by providing senior review of study level/program level/multi study core deliveries for accuracy.
Attends sponsor audits and assists with in-progress audits.
Monitors scope of work to actual work, alerting management of potential change orders; manages and executes the change order to completion.
Monitors applications for workflow alerts, system errors, and performance issues.
Performs system integration activities, application updates, and user acceptance testing.
Attends Quick Start Camps (QSCs) as the lead clinical programmer for assigned studies.
Leads clinical programming activities.
Travel: Roving/Telecommuting Employee: Reports to company headquarters in Raleigh, NC. Will work at various unknown client sites throughout the U.S. for up to 100% of the time. Must be willing to travel anywhere in the U.S. and may be assigned to work at client sites across the U.S. Can work remotely or telecommute.
Qualifications: Master s degree in Biology, Biotechnology, Mathematics, Statistics, Computer Science, Engineering or related field of study plus 3 years of software development, programming or related experience. Employer will also accept a Bachelor s degree plus 5 years of experience as an equivalent alternative.
Special Skills: Demonstrated knowledge or experience with:
Clinical Data Management;
Relational database development, Electronic Data Capture and reporting;
Oracle RDC, Oracle Inform;
Medidata Rave, OmniComm TrialMaster;
To apply, submit resume to: https://incresearch.taleo.net/careersection/ex/jobsearch.ftl*lang=en, Ref Job title: Senior Clinical Programmer