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Senior Statistical Programmer (South America)

Names the CaribbeanCaribbean hours OK
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✓ Screened eligible

Why you can actually get this job

The posting explicitly lists Guyana in the source-provided allowed countries and includes UTC-5 in the permitted timezone offsets, which matches the target user's location and timezone. The role is for South America with no language requirement beyond English stated, and no work authorization restrictions are mentioned.

“Argentina, Bolivia, Brazil, Chile, Colombia, Ecuador +6 more” Geographic scope — Caribbean named explicitly; included subject to G3 (which passed above).
“suriname” Geographic scope — Structured location list contains unrecognisable entries — templated artifact, not trusted as scope.
“Source-provided allowed countries: Argentina, Bolivia, Brazil, Chile, Colombia, Ecuador, Guyana, Paraguay, Peru, Suriname, Uruguay, Venezuela” Geographic scope — Guyana is explicitly named in the allowed countries list, confirming the role is open to anglophone Caribbean jurisdictions.
“Source-provided allowed UTC offsets: -6, -5, -4, -3, -2” Timezone — UTC-5 (Jamaica/Caribbean timezone) is included in the permitted offset range, satisfying timezone overlap requirements.
“Excellent communication skills.” Language — No language beyond English is required; communication skills are stated generically without specifying Spanish or bilingual fluency.

About the role

The Bioforum Biometrics department is growing, and we have an opportunity for an experienced statistical programmer to join our group. This position is in Latin America (South America).

Required skills

  • Minimum 6 years’ experience as a statistical programming working on clinical trials.
  • Good knowledge of TFL programming.
  • Experience in programming according to CDISC standards (SDTM, ADaM), and preparing documents for submission (Reviewer’s Guide, Define.xml)
  • Attention to details.
  • Excellent communication skills.
  • A bachelor’s degree in either statistics , computer or life science discipline

Duties will include

Participating in all statistical programming activities including preparing clinical data to submission using CDISC or customized standards, reviewing data conversions, data analysis datasets and outputs and taking part in creating best practices and implementation guides.

  • Might need to be responsible for project management (timelines, scope, budget, resourcing) on a project or program level.
  • Train, mentor and share knowledge with the rest of the statistical programming team.
  • Creating programming specification documents for all types of data (SDTM, ADaM, Derived data, etc.).
  • Might include Interaction with customers on a project or program level.
  • Development of SAS programs for conversion of the clinical data based on CDISC or customer instructions.
  • Development of SAS programs for analysis datasets based on SAP, shells and CDISC or customer instructions.
  • Development of SAS programs for study TFLs, based on study SAP and shells.
  • Review and verify all types of conversions and programming done based on customer requirements.
  • Development of core programs for validation, conversion, and maintenance of clinical data dataset structure.
  • Follow the appropriate Standard Operating Procedures (SOPs) for all statistical programming related activities.

Originally posted on Himalayas

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Opens the original posting, where you apply.

At a glance

  • EmploymentNot stated in posting
  • Hiring scopeArgentina, Bolivia, Brazil, Chile, Colombia, Ecuador, Guyana, Paraguay, Peru, Suriname, Uruguay, Venezuela
  • Time zoneCaribbean hours OK
  • SalaryNot disclosed
  • Posted1mo ago

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