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Job Description
Position Overview
Under the direction of the Associate Director/Manager, the Programmer will set up Data Collectors/Reports in support of clinical data management activities
Assumes the responsibilities for all Reporting deliverables in support of the clinical studies.
Coordinates and participates in the following activities
Design, build, maintain, test, and document reports based on written specifications established by Global Clinical Data Management, Clinical Research and Global Safety.
Review the technical feasibility of study team proposed reports and technically implements them.
Qualifications
Knowledge and Skills
Experience in SQL, PL-SQL
Advanced English level
Solid knowledge of MS Windows/Office software and exposure to web based applications.
Solid knowledge of System Development Lifecycle Management / system validation knowledge
Ability to establish and maintain good working relationships with different functional areas.
Strong sense of urgency and customer focus.
Strong organizational and problem-solving skills.
Desire and ability to learn new processes and technologies
Ability to multi-task, work independently, and good communication skills
Desired experience in SAS, JReview and COGNOS
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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