PRAHS 2018-45380 in United States

Responsible for successfully providing data management deliverables that meet internal and external client needs.

  • Manages access within the clinical database, including creation, modification, and revoke of access for personnel

  • Create the annotated case report form (aCRF) based upon the protocol

  • Review, revise and create processes for established and for the Clinical Data Management SOPs and Guidelines

  • Assist with maintenance of all relevant documentation associated with each assigned Protocol.

  • Build studies within clinical database using the related study documentation

  • Perform required testing within the clinical database

  • Perform and/or oversee database validation including generation of scripts, reports, execution of validation, and related documentation

  • Program edit checks within clinical database

  • Maintain the clinical database throughout the study

  • Ensure that appropriate study documentation related to the clinical database is filed

  • Provide database programming support for ad hoc listings and reports to Clinical Data Management staff

  • Provide assistance, mentoring, and/or training to Clinical Data Management staff as necessary.

  • Interact with various Data Management and other functional area colleagues, including, but not limited to: Information Services, Information Technology, Biostatistics and Programming, Clinical, Project Management, Safety, Medical Coding, site personnel.

  • 3-5 years of data management experience required

  • Bachelors degree preferred, but not required

  • Database build and maintenance required

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

ID: 2018-45380

External Company Name: Pharmaceutical Research Associates, Inc

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