Pop Science is a recruitment-process outsourcing & staffing consultancy specialising in the supply of scientific and clinical development staff to clinical trials and technology industries.
We promote research and career development in science and innovation. Pop Science has, collectively, over 30 years’ experience in this field.
Each of our consultants has worked directly within the industry which makes us unique as we have first-hand experience and understanding in the roles that we handle.
Pop-Science is pleased to bring to the market a role of:
CONTRACT Senior SAS Programmer
Type: 6 month Rolling Contract
Location: Home Counties
Rate: Up to £50 per hour DOE
Full time Office Based
A contract SAS Programming role with a pharmaceutical client based in the south east UK, working within the Oncology therapy area.
In this role you will support the Biostatistics team by providing timely production and validation of high quality statistical programming deliverables for Clinical Studies Reports, integrations, submiision activities, exploratory analyses and regulatory requests. You will contribute to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.
In this role you will:
- Produce and validate high quality statistical programming deliverables (SDTMs, ADaMs, Tables, Listings and Graphics)
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Support objectives, policies and operational targets that have a direct impact on the work unit or operational outcom
- Review the SAP, provide feedback to the statistician and develops (with the statistician) study specific datasets
- Develops programs for the creation and validation of datasets (SDTM & ADaM) and TLGs
- Integrates multiple studies in support of an ISS/ ISE.
- Supports ad-hoc, interim, exploratory, publications and performs programming and generates outputs
- Maintains data, programs and reports in accordance with 21 CFR part 11
Qualifications and Experience
- BS or MS in Relevant Field
- Experience in clinical development statistical programming methods and processes in industry setting required
- Working experience with SDTM and ADaM, preferably in the area of Oncology studies including submission supports and related training
- Experience using SAS-Base, MACRO, SQL, STAT, GRAPH, MS Office.
- Proven experience with Windows operating systems.
- Understanding of the software development life cycle.
- Understanding of FDA guidelines.
- Good organisation, time management and attention to detail skills needed
- Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment
You must be eligible to work in the EEA.
best wishes
Helena Newman-Mitchell