Junior Statistical SAS Programmer

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Solo per membri registrati
Ferrara
EUR 35.000 - 55.000
Sii tra i primi a mandare la candidatura.
5 giorni fa
Descrizione del lavoro

The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is primarily responsible for developing SAS programs to generate datasets, tables, figures, and listings for clinical studies (per ICH E3), publications, or Health Authorities requests. The role involves collaboration with Biostatistics and Data Management teams on clinical trials and projects.

Key Responsibilities include:

  • Developing SAS programs for datasets, tables, figures, and listings for clinical trials, publications, and Health Authorities requests.
  • Using CDISC guidelines to generate SDTM and ADaM datasets.
  • Writing programming specifications for analysis datasets.
  • Validating ADaM datasets using Pinnacle 21.
  • Preparing, maintaining, and archiving CDISC documentation such as Define.xml and ADRG.
  • Developing standard SAS macros and validation documents.
  • Liaising with Data Management to develop SAS programs, macros, and utilities to identify data discrepancies.
  • Handling external clinical data, developing SAS programs for import and reconciliation.
  • Developing and validating SAS programs to identify Non-Protocol Deviations.
  • Collaborating with Biostatistics and Data Management teams on clinical projects.
  • Maintaining SAS programming documentation.
  • Contributing to the development and maintenance of SOPs, templates, and programming standards.
  • Staying informed on new SAS developments relevant to clinical data management.
  • Ensuring KPI and metrics for studies are met.
  • Completing required trainings on time.
  • Accurately entering data into the TRACK system daily.
  • Performing additional tasks as assigned.

Qualifications:

  • At least 1 year of experience in CRO, biotech, pharma, or research institutes in a similar role is preferred.
  • Knowledge of HA requirements related to pharmaceutical research and SAS programming.
  • Understanding of statistics and its application to clinical trials.
  • Proficiency in SAS and CDISC standards (SDTM, ADaM).
  • Strong planning and organizational skills.
  • Team-oriented mindset.

What We Offer:

Competitive salary, bonuses, and benefits, along with opportunities for professional growth within an expanding international company.

Please review the candidate data processing notice on our website.

About Us:

OPIS is a 25-year-old international CRO providing comprehensive clinical research services worldwide, including drug trials and medical device studies, utilizing cutting-edge technology and innovative approaches.

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