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.
External Company Name: Pharmaceutical Research Associates, Inc
External Company URL: http://prahs.com/