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SR Statistical Programmer

Role overview

Qualifications

  • Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.
  • Experience and/or education plus relevant work experience, equating to a Bachelor's degree.
  • Typically, 3-5 years of SAS® programming experience in the CRO or Pharmaceutical industry.
  • Knowledge of CDISC requirements.

Responsibilities

  • Perform the role of the Lead Statistical Programmer.
  • Plan, execute and oversee all programming activities on a study.
  • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs.
  • Mentor less-experienced programmers in the processes around SDTMs, ADaMs and TFLs.

Key facts

  • Remote from: Brazil
  • Full time
  • Senior (5-10 years)
  • English

Hard skills

Other skills

  • Time Management
  • Mentorship

About the company

Fortrea logo

Fortrea

Contract Research Organizations (CRO)

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

Summary of Responsibilities:

  • Perform the role of the Lead Statistical Programmer.
  • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality,
  • interaction with other departments and the client, etc.
  • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform QC of SDTM, ADaMs and TFLs.
  • Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated CRFs and Reviews Guides to support SDTMs and ADaMs.
  • Develop specifications for SDTMs and ADaM datasets.
  • Review SAPs and TFL shells from a programming perspective for studies.
  • Mentor less-experienced programmers in the processes around SDTMs, ADaMs and TFLs.
  • Present and share knowledge at department meetings.
  • Respond to QA and client audits, and support qualification audits.
  • Identify processes within programming that will increase productivity, quality, and efficiency.
  • All other duties as needed or assigned.

Qualifications (Minimum Required):

  • Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.
  • Experience and/or education plus relevant work experience, equating to a Bachelor's degree.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
  • Language Skills Required: Speaking: Yes, English required Writing/Reading: Yes, English required

Experience (Minimum Required):

  • Typically, 3-5 years of SAS® programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
  • Knowledge of CDISC requirements.

Physical Demands/Work Environment:

  • Office or home-based environment, as requested by the line manager.
  • Travel Requirements: Yes.
  • Local, Domestic, Regional.
  • % of time: Approximately 5%.
  • % of the above that requires overnight stay: Approximately up to 100%.
  • Travel is primarily to where: client meetings and trainings.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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