Clinical Data Programmer Analyst(12395)

Location: Hamilton, Ontario, Canada
Date Posted: 19-09-2018
One of our top clients in the Hamilton region is looking to hire an Intermediate level Programmer Analyst to support their Biometric/Clinical Data tracking application. This exciting opportunity is being offered as a 1 year contract opportunity with the potential for further extension and/or full-time. 

As the Programmer analyst, your role will be to ensure accurate design, implementation and maintenance of clinical research databases in accordance with study specifications. Coupled with the development of new forms and the validation of edit/checks, the Programmer Analyst will ensure good database design and data management standards and organizational procedures that support the accurate analysis of study data essential to meet the scientific goals and research. 

Job Accountabilities:
  1. Implement eCRF and/or edit check design and ad-hoc tools to support study requirements and ensure accurate data collection.
  2. Apply appropriate methodology used in clinical trial data management to the data capture system in order to ensure the completeness, accuracy and consistency of the data collected.
  3. Prepare and validate listings and reports using clinical reporting and business intelligence tools to support the conduct of the study and the quality of the data.
  4. Prepare and validate accurate data sets for statistical reporting and analysis.
  5. Prepare and validate secure data transfers of clinical data to internal and external parties.
  6. Define, prepare and execute test specifications for validation purposes.
  7. Comply with good database design and programming standards as well as all organizational procedures.
  8. Review and provide input to study data management plans, specific study protocols and case report forms for implications that will affect the eCRF and/or edit check design and implementation.
  9. Develop and maintain data management and programming documentation following organizational procedures.
  10. Maintain working knowledge of internal systems to generate project work.
  11. Manage and work independently on multiple concurrent projects with supervision of senior staff.
 
Qualifications:
  1. Undergraduate Degree in Computer Science, Statistics or related field.
  2. Strong skills in Computing Science or Statistics
  3. Minimum 3 years’ experience in a health related biometric and/or data management field.
  4. Experience with cdash and/or omnicomm trialbuilder and trialmaster
  5. Thorough knowledge in developing and maintaining SAS and/or other analytic applications.
  6. Thorough knowledge of relational database management systems (e.g. Oracle, SQL)
  7. Knowledge of any of the following common programming languages: C, Python, JavaScript, etc.
  8. Proficient in a UNIX environment.
  9. Ability to work independently and in a collaborative team environment.
If you feel that you have the required experience, technical skill set, and are looking to work on a longer term assignment on an amazing team for one of the country's most prolific clinical research institutions, please apply immediately as this role will not around for long. 
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