Clinical Programmer (Senior), FSP - South Africa at Parexel
Home Based, , South Africa -
Full Time


Start Date

Immediate

Expiry Date

10 Nov, 25

Salary

0.0

Posted On

11 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Reporting, Sql, Sdtm, Statistics, Clinical Data, Teams, Communication Skills, Excel, Life Sciences, Mathematics, Microsoft Products, Etl, Outlook, Programming Languages, Computer Science, Software, Cdisc Standards, Data Integration

Industry

Pharmaceuticals

Description

SKILLS REQUIRED:

  • Skilled in programming in a relational database setting with SQL and/or T-SQL or ETL.
  • Ability to balance and prioritize multiple assignments and respond quickly to ad hoc requests.
  • Familiarity with CDISC standards, including CDASH and SDTM.
  • Excellent verbal and written communication skills.
  • Project management skills an advantage.

EDUCATION REQUIREMENTS:

  • Bachelor’s degree in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields
Responsibilities

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Essential Knowledge and Experience Required for this role:

  • Minimum of five years of experience in developing software in a clinical trial environment using SQL, including at least three years of clinical programming experience.
  • Experience with data reporting tools in a clinical trial setting.
  • Experience in the Biotechnology, Pharmaceutical, or Life Sciences industries (Clinical Research Organization - CRO or Clinical Trial regulated environment preferred).
  • Experience with the eClinical Solutions elluminate platform an advantage.
  • Knowledge of some additional programming languages (e.g.: SAS, PL/SQL, R, Python, Java, …) a definite advantage.
  • Experience with Qlik Sense a plus.
  • Preferred additional external data transfer experience in:
  • Creating external data transfer specifications, ensuring external clinical trial data are compatible with the clinical database to support data integration, analysis and reporting.
  • Experience in planning, set-up, and acquisition of external clinical data at the study level
  • Liaising with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.).
  • Working knowledge of Microsoft products: Outlook, Word, Excel, Teams.
  • We may have flexibility to hire at either Senior Clinical Programmer level or Junior Clinical Programmer level for this role. Junior level experience requirements include up to five years of relevant experience and Senior level positions would require five or more years of relevant Clinical Programming experience
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