inVentiv Health Clinical-Sr.clinical Data Management Programmer -k

Careers Save this JobApply Button will redirect you to recruiters resume management system Report this job inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing. Designation Sr.clinical Data Management Programmer Job Description Perform the duties of a Clinical Data Management System (CDMS) support specialist to ensure minimal downtime and quick problem resolution: Troubleshoot CDMS errors Instruct other Data Management staff in the proper use of CDMS Report suspected CDMS problems to the vendors user support group Implement or ensure the implementation of any necessary fixes to CDMS Report suspected Oracle problems to PharmaNet Oracle Database Administrator May perform some or all of the following tasks: Act as CDMS database administrator by providing new user accounts, user groups, updating user groups and system parameters Train programming staff on data management procedures and systems Create an annotated CRF using PharmaNet standards or sponsor requested naming conventions Create and test the CDMS set up for new studies/projects Create and test data entry screens, write data entry guidelines Program and test the automated edit checks to be executed for the study/project Create and test files necessary for the electronic upload of data Upload electronic data received through external sources (e.g., central laboratories) Communicate the database set-up status and the achievement of milestones to internal or external project team members Update PharmaNet standard data dictionaries and edit check libraries Program and generate data listings for ongoing studies Program and generate project tracking reports Ensure archiving of electronic data and required documentation is effected on study completion Program CDMS enhancements Coordinate and participate in the validation of a CDMS or related supporting software Write materials or perform technical training for Data Management staff Desired Profile Bachelors Degree, preferably in Computer Science In lieu of a Bachelors Degree, completion of a certified relational database training program/course work or related web development program/course work, and six years (total) of relevant experience in data management or system validation Three years of relevant database programming in Rave programming or system validation experience including one year in data management Competency in Rave database programming or system validation Ability and willingness to travel on occasion Experience 5 - 8 Years Industry Type Pharma / Biotech / Clinical Research Role Clinical Research Associate/Scientist Functional Area Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology Education UG - Any Graduate - Any Specialization PG - Any Postgraduate - Any Specialization DOCTORATE - Any Doctorate - Any Specialization, Doctorate Not Required Location Hyderabad / Secunderabad, Pune, Mumbai Keywords Clinical Data ProgrammerRave progarmmer Contact Colin inVentiv International Pharma Services Pvt Ltd Job Posted 13 Sep Save this JobApply Button will redirect you to recruiters resume management system Report this job