PRAHS

2017-40627

- | US-KS-Lenexa
12 hours ago
Title
Database Programmer- Oracle Clinical

Overview

Database Programmer

Location – Lenexa, KS

Overview:

 

Creates and maintains database infrastructure for the collection of clinical data according to PRA and/or client Standard Operating Procedures (SOPs). This includes the design, implementation and validation of databases, edit checks, import/export of external data, and knowledge of SDTM deliverables.

 

 

 

 

Responsibilities

Requirements:

  • Perform billable work in accordance with PRA’s policies and standard operating procedures (SOPs) to provide consistent high quality deliverables
  • Familiarity with the study protocol
  • Define databases and data entry screens for clinical trials
  • Program edit checks for clinical databases based on the Data Validation Plan
  • May create paper source documents for clinical trials, including label
  • Import non-case report form (CRF) data into the clinical database as described in the Data Transfer Agreement and/or SOPs
  • Reconcile non-CRF data with data from the CRF
  • Create appropriate sections in the Data Transfer Agreements
  • Review and approve database definitions for clinical databases and edit checks
  • May assist in the creation and QC of conversion programs
  • May create annotated CRFs
  • May create SDTM define.xml
  • Assists in the locking of study databases (import external data, extraction of final data from database)
  • Assist in the training of junior Database Programmers
  • May attend sponsor meetings, as required
  • May assist in communication with vendors as it relates to data imports 

Must Have:

  1. Must be an in office employee (or at least 4 days in office)
  2. Must have at least 2 years of Oracle Clinical Programming from CRO or Pharma

 

Willing to Consider:

  1. Remote if 5 or more years Oracle Clinical programming from CRO or Pharma
    • Top notch communicator over the phone
    • Willing to come to the office for 1 week training (initial)
    • Willing to come to the office 3-4 days every 3 months

 

Qualifications

Qualifications:

  • Read, write and speak English; fluent in host country language required.
  • Minimum of two years industry related database programming experience required
  • Minimum of two years of experience with Oracle, SQL, PL/SQL, and/or SAS required
  • Experience with clinical trials or the pharmaceutical industry
  • Knowledge of data structure standards (CDASH, SDTM) preferred
  • Demonstrated ability to successfully interact with internal clients and related department/functions.
  • Knowledge with programming in SAS and working with EXACT preferred
  • A bachelor’s degree in a quantitative or scientific field, or its international equivalent from an accredited institution.
  • Programming on Oracle Clinical preferred
  • Experience with industry standard clinical data management systems preferred
  • Experience as primary representative of clinical data management project team preferred

 

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

Options

Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed

Connect With Us!

Not ready to apply? We get it! Click here to stay in touch for future opportunities, events and other happenings!