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Senior Statistical Programmer

72% Flex
UNLIMITED HOLIDAYS - EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE - LONG REMOTE PERIOD ALLOWED
Remote: 
Full Remote
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

10-15+ years of statistical programming experience in pharma/biotech, Experience with SDTM, ADaM specifications, TFLs, regulatory submissions.

Key responsabilities:

  • Support statistical programming activities for clinical studies and maintain standards
  • Manage CROs, review deliverables, and execute statistical programming tasks for multiple studies
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
See more Katalyst HealthCares & Life Sciences offers

Job description

Logo Jobgether

Your missions

Responsibilities:
  • Support statistical programming activities for clinical studies, ensure statistical programming deliverables are delivered within timelines.
  • Maintain statistical programming standards, processes, and SOPs.
  • Manage CRO and review deliverables for accuracy and compliance, performing acceptance check and validation.
  • Manage, review, and/or execute statistical programming deliverables for planned statistical analysis related to study monitoring, clinical study reports, data integrations, and regulatory query responses, covering multiple studies.
  • Generate TFLs to support ad hoc requests.
  • Review data management documents (CRF specification, data transfer agreements, DMP, annotated CRF), SDTM and ADaM specification, SAP, and TFL shells to provide statistical programming feedback.

Requirements:

  • 10-15+ years of statistical programming experience in the pharma/biotech industries.
  • Must be able to independently develop SDTM and ADaM specifications (DDT) and program, develop and validate TFLs.
  • Recently creating define.xml using Pinnacle 21 Enterprise.
  • Must have recent experience supporting regulatory submissions.
  • Define package experience and ISS/Client experience.
  • Strong experience with regulatory submissions activities (BLA/NDA).

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

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