Clinical Programmer III Medidata Rave
Theorem Clinical Research - Pennsylvania

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− University/College degree or relevant experience.
− 5+yrs.CDM.
− Some travel.
− Produces high quality work using SOPs, guidelines and technical standards as defined by the global technical group.
− Keeps others informed of project and/or technical issues by pro−actively communicating across teams/functions.
− Manages time effectively in order to produce a quality deliverable in expected timeframe.
− Completes all tasks agreed upon with minimum supervision.
− Anticipates changing priorities and demands and addresses them proactively.

Job Description:
JOB SUMMARY
Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented
problems in a timely manner, as appropriate for the position.

JOB RESPONSIBILITIES
− Be familiar with, and/or have experience and understanding of all tasks and responsibilities associated with Programmer I and II
− Have the technical knowledge and provide guidance on providing interfaces or data exchanges between the Clinical database and
other database, programming or reporting systems. Be able to export data or allow views of data from the Clinical database to other
computer systems in a secure and verifiable method. When necessary provide support for tools which require access to the clinical
database
− Have the ability to load large scale external data or entire databases into the Clinical database. To provide technical support, project
process and determine resource requirements necessary to perform such duties as described above
− Be able to use and support the many software products used with the clinical database package. This would include, but not be limited
to, Thesaurus management systems, reporting systems and packages, autoencoding packages and remote data capture interfaces
− Have to ability to perform problem solving and troubleshooting for system procedures and processes that may arise in course of a
clinical trial as related to the clinical database
− If necessary, to assist with statistical reporting procedures following the Biometrics departments SOP’s and guidelines.

KEY SKILLS & BEHAVIORS
− Produces high quality work using SOPs, guidelines and technical standards as defined by the global technical group.
− Keeps others informed of project and/or technical issues by pro−actively communicating across teams/functions.
− Manages time effectively in order to produce a quality deliverable in expected timeframe.
− Completes all tasks agreed upon with minimum supervision.
− Anticipates changing priorities and demands and addresses them proactively.

TRAINING AND EXPERIENCE
− University/College degree or relevant experience.
− 5+yrs.CDM.
− Some travel.

Theorem Clinical Research - 2 years ago - save job
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Theorem Clinical Research is one of the foremost providers of comprehensive CRO services with offices in more than 30 countries and a...