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Data Transformation Programme Lead
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Data Programmer
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Data Programmer
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Data Programme Manager
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Altum Consulting London, United Kingdom Full timeData Programme Manager · Salary: £80,000 · Location: London (Hybrid) · Contract type: Permanent · Altum Consulting are pleased to be working with a renowned Housing Association who are on the search for a well rounded Data Programme Manager to lead a priority programme. The pos ...
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Data Programme Manager
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SAS Data Programmer
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Warman O'Brien United KingdomSenior Statistical Programmer | Pharma | Fully Home Based | UK | · Warman O'Brien are working with a Global Pharma who due to continued success and growth in the UK, have several opportunities for experienced Senior Statistical Programmers to join them. As a Senior Statistical Pr ...
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Data Programme Manager
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Bumble Inc. London, United KingdomInclusion at Bumble Inc. · Bumble Inc. is an equal opportunity employer and we strongly encourage people of colour, lesbian, gay, bisexual, transgender, queer and non-binary people, veterans, parents, people with disabilities, and neurodivergent people to apply. We're happy to m ...
SAS Data Programmer - United Kingdom - Cytel - EMEA
Description
At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful.
Position is home-based in Europe (UK, Germany, France, Spain)We are experiencing exponential growth on a global scale and hiring Senior Statistical Programmers to join our FSP division.
You will apply your know-how in CDISC standards (SDTM & ADaM) and advanced SAS programming skills, tosupport or lead one or more Phase I-IV clinical trials, across a variety of therapeutic areas.
We believe in applying scientific rigor to reveal the full promise inherent in data.~ We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
~ As a Senior Statistical Programmer , you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
Generating and validating analysis datasets/analysis files, and complex tables, listings, and figures ( TLFs)
Production and QC / validation programming
Generating complex ad-hoc reports utilizing raw data and analysis datasets
Applying strong understanding/experience of Efficacy analysis
Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
Being adaptable and flexible when priorities change
Generating and validating Non-CDISC transformation datasets and analysis datasets
Individuals should be able to start programs from scratch and have the ability to handle complicated domains and outputs related to the protocol and SAP.
They must demonstrate a good understanding of the endpoints and data collection, with the ability to read and write specifications related to the respective implementation guides.
R & complex macro writing are a plusBachelor's degree in one of the following fieldsStatistics, Computer Science, Mathematics, etc.
At least 8years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industrywith a bachelor's degree or equivalent.
At least 6years of related experience with a master's degree or above.Study lead experience, preferably juggling multiple projects simultaneously.
Strong SAS data manipulation, analysis and reporting skills.
Strong QC / validation skills.
Good ad-hoc reporting skills.
Proficiency in efficacy analysis and survival analysis
Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
xml and other submission documents
Ability to provide quality output and deliverables, in adherence with challenging timelines.
Our collaborative working environment encourages innovation and rewards results, and we are proud to have one of the lowest turnover rates in the industry.
In addition to a competitive compensation, we offer an excellent benefit's package, annual bonus incentive, promote work-life balance, and the opportunity to grow with usWork with respected experts and thought leaders in the fields of biostatistics and statistical programming.
Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
Visit this company's hub to learn about their values, culture, and latest jobs.
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