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Statistical Programmer - SAS & R Experience

Remote: 
Full Remote
Contract: 
Salary: 
38 - 38K yearly
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Degree in mathematics, life sciences, or similar, Solid programming experience with R and SAS, Experience with SDTMs, ADaM datasets, and TFLs, Knowledge of CDISC standards, Fluency in English, both spoken and written.

Key responsabilities:

  • Review SAPs and TFL shells from a programming perspective
  • Develop complex specifications for SDTM and ADaM datasets
  • Maintain SAS programs for dataset creation and quality control
  • Produce XML/PDFs and support documentation
  • Propose improvements for efficiency and quality in programming
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Job description

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

As a Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies.

In this role, you will develop and validate SAS and R programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team.

This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as chronic and rare diseases. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!

In this role, programming experience in R and SAS is required.

In this role, you can be 100% home-based or you can work from our local offices.

What else can you expect from us?

  • Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
  • Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
  • A genuine work life balance
  • Flexibility in working hours
  • A thorough onboarding with support from your personal mentor
  • A permanent employment contract with Fortrea
  • Excellent training and career development opportunities, as well as support with advancing your individual education
  • Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide

Your responsibilities:

  • Review SAPs and TFL shells from a programming perspective
  • Advise on the development of complex TFL shells from a programming perspective
  • Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets
  • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs
  • Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
  • Respond to QA and client audits and support qualification audits
  • Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business
  • Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs)

Your profile:

  • Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
  • In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials
  • Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company
  • Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs
  • Programming experience in R is required
  • Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs
  • Solid knowledge of CDISC standards
  • Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail
  • Business fluency in English both spoken and written is a must

Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/974d5f9c95f62f7bec3ffb384b5d3fee

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Information Technology & Services
Spoken language(s):
EnglishEnglish
Check out the description to know which languages are mandatory.

Other Skills

  • Quality Control
  • Collaboration
  • Creative Problem Solving
  • Organizational Skills
  • Detail Oriented
  • Mathematics

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