Statistical Programmer II - Sponsor Dedicated

Fortrea; Thatcham; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading pharmaceutical company is seeking a Statistical Programmer II to deliver complex clinical trials for top pharmaceutical clients. The role allows for 100% home-based work, or use of local offices. Candidates should possess a Bachelor's degree and 1 - 2 years of SAS programming experience in the CRO or pharmaceutical industry. Key responsibilities include leading programming activities and developing SAS programs for SDTM and ADaM datasets.

Qualifications

• Minimum Bachelor's degree in a relevant field.
• 1 - 2 years of SAS programming experience in the CRO or Pharmaceutical industry.
• Knowledge of CDISC requirements is essential.

Responsibilities

• Assume the role of a Lead Statistical Programmer for CP studies.
• Plan, execute, and oversee all programming activities.
• Develop and maintain SAS programs for SDTM and ADaM datasets.

Skills

SAS programming experience

Knowledge of CDISC requirements

Business fluency in English

Education

Bachelor's degree in mathematics, statistics, computing, or related fields

Job description

Overview

As a Statistical Programmer II 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. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.

You can be 100% home-based or if you prefer, you can work from our local office in your home country.

Responsibilities

• With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff.
• 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 eCRFs and Reviews Guides to support SDTMs and ADaMs.
• With support from senior programming staff, develop specifications for SDTMs and ADaM datasets.
• Review SAPs and TFL shells from a programming perspective for studies with support from senior programming staff.
• Respond to QA and client audits with support from senior programming staff.
• And all other duties as needed or assigned.

Qualifications

• Minimum Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.
• Typically, 1 - 2 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.
• Business fluency in English - both spoken and written - is a must.

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