Clinical Programmer

Description:

Responsible for creation of Analysis Datasets, tables, figures, listings and insuring the accuracy of project /study level output. Responsibilities include production of reports to facilitate the collection and cleaning of clinical trial data. The role will include tasks such as:

	Develop and produce regular reports to meet specific project deadlines
	Run current data checking software and develop further sense checks in collaboration with the project team
	Support detailed data monitoring activities, answer specific questions on the clinical database keeping the interpretability and presentation of the final data in mind

This role requires identification of the general cause of any reporting issues (e.g. data or programs) and their possible resolution with data management, programming, statistical or clinical staff as appropriate.

Requirements:

This position requires a bachelors degree or higher in computer science, statistics or a related field plus three to four years experience in database design, two years experience in SQL and 2 years of exposure to government regulated industries. Experience in programming clinical systems for clinical trials, formal SAS training and experience in SAS programming is preferred.

To apply for one of the above positions, please submit your résumé or curriculum
vitae (CV) to careers@researchpoint.com

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