Clinical Database Programmer II

October 4

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• The Clinical Database Programmer II provides technical expertise for the conduct of clinical trials. • Works with minimal supervision to support various programming activities related to clinical systems. • Responsible for eCRF design, edit check programming, and validation. • Create, implement, and maintain database set-up for clinical data management systems (CDMS). • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines/Work Instructions. • Participate in the creation of standards for efficient processes.

Requirements

• Good English written and oral communication skills. • Demonstrate ability to learn new systems and function in an evolving technical environment. • Attention to detail. • Ability to work together with a team (including international teams as required) as well as independently. • Work effectively in a quality-focused environment. • Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change. • Business/Operational skills that include customer focus, commitment to quality management and problem solving. • Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICHGCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application. • Experience in at least one programming environment (e.g. SAS, CDMS, EDC, SQL, VB, Java).