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Vacancies for Database Programmer II @ PPD

Job Description

Database position working with clinical trials data systems under general supervision. Designs and implements global library and study specific setup for clinical trials applications; develops and validates data checks; provides first-line end-user support/problem solving; provides support for application validation activities

Functions and Responsibilities:
Participates in Study specific database design / build activities
Reviews designs for compliance/feasibility within the database system and
consistency with any current standards and/or sponsor specifications. Seeks input and guidance from Technical leads and managers when necessary.
Meets with study teams on a regular basis during initial study setup to ensure
effective communication and accuracy in design
Under supervision and guidance from Technical Operations leads and managers,
designs, annotates and builds databases and develops/validates data checks within the timelines established by the team and indicated by the contract.
Updates annotations and production databases where required based on protocol amendments or other changes to trial designs within a reasonable time period.
Performs core setup and supports processes for various peripheral systems
Understands and follows departments working practice documents and SOPs, and contributes to their development as needed.
Understand and follows appropriate corporate SOPs.
Provides general support to Technical Operations Department
Participates in Study specific database design / build activities
Reviews designs for compliance/feasibility within the database system and
consistency with any current standards and/or sponsor specifications. Seeks input and guidance from Technical leads and managers when necessary.
Meets with study teams on a regular basis during initial study setup to ensure
effective communication and accuracy in design
Under supervision and guidance from Technical Operations leads and managers, designs, annotates and builds databases and develops/validates data checks within the timelines established by the team and indicated by the contract.
Updates annotations and production databases where required based on protocol amendments or other changes to trial designs within a reasonable time period.
Performs core setup and supports processes for various peripheral systems
Understands and follows departments working practice documents and SOPs, and contributes to their development as needed.
Understands and follows appropriate corporate SOPs.

Minimum Required Education and Experience:

Bachelors degree in computer science, statistics, biostatistics, mathematics, biology or other health related field or equivalent experience that provides the skills and knowledge necessary to perform the job.
4-7years of experience with data collection or analysis, or working with relational databases in a clinical research or clinical drug development environment
Rave Programming with Custom Function experience, edit check.

Required Knowledge, Skills and Abilities:
Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.
Good computer skills
Knowledge of relational database systems (RDBMS) and structure
Strong attention to detail and problem solving skills
Good written and verbal communication skills
Ability to maintain a high degree of confidentiality with clinical data and clients proprietary data
Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPs
Positive attitude, enthusiasm toward work, and the ability to work well with others.

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