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Clinical Programmer

Pyramid Consulting, Inc.

This is a Contract position in Berkeley Heights, NJ posted June 22, 2020.

Immediate need for a Job title Clinical Programmer experience in the Pharmaceutical Industry. This is 6 Months Contract position with possible extension located in Berkeley Heights, NJ. Please review the job description below JOB ID 20-17872 Responsibilities will include, but are not limited to Oversee and monitor CRO DB Build (in Medidata Rave) to ensure that Client standards are implemented in all studies Schedule and lead eCRF design meetings Routinely interface with cross-functional team members Proper management of project priorities and timelines required Review clinical programming activities and costs in contracts Develop, program, test and maintain clinical trial databases and data entry screens using Medidata Rave in accordance with Client standards Review validationedit checks for in-house and outsourced studies Act as liaison with vendors and oversee CRO to establish external data transfer specifications Retrieve data from CRO and external vendors. Develop, program, test and maintain data review listings in Jreview andor SAS for data review purposes Provide technical expertise and support to Data Management team Make data available to company personnel and regulatory agencies when required Perform post processing of data extracts in accordance with Client standards to be delivered to Biostatistics (if in-house study) Coach and advise junior programmers to identify problems and solutions KNOWLEDGESKILLSABILITIES (KSArsquos) – in order of importance BSBA degree or equivalent in a relevant scientific discipline with a minimum of five years experience Detailed knowledge and experience in case report form design, central laboratories, programming databases, query resolution, data validation Advanced knowledge of clinical database design is a must (Medidata Rave experience is most important. Inform and Oracle Clinical or other systems are of lesser importance). Good communication skills is a must Ability to work in a team environment with data managers, medical personnel, clinical monitors, statisticians, programmers, and medical writers Knowledge of FDAICH guidelines and industry standard practices regarding programming Medical or mathematicscomputer science background a plus Knowledge of SQL and SAS programming Knowledge of clinical trial design and basic statistics (a plus) Our client is a leading Pharmaceutical Organization and we are currently interviewing to fill this and other similar Contract positions. Qualified candidates should apply online for immediate consideration.