Job Details
Clinical Programmer - FSP
5037
Posted: 21/12/2024
- £Competitive
- Home Based, United Kingdom
- Permanent
Clinical Programmer | Pharma | Permanent | UK / Europe | Home Based |
A leading global CRO is offering an exciting opportunity for a Clinical Programmer to join their team. In this role, you will work exclusively with a prestigious global pharmaceutical client that values excellence, rewards achievement, and prioritizes quality. The company fosters an environment of innovation and individuality, welcoming professionals eager to contribute to its dynamic culture. This position is fully remote and open to candidates based in the UK or other locations across Europe.
What you will be doing:
You will need to have:
What you’ll receive:
Apply now or contact Jo Fornaciari at +44 7488 822 859 / jo@warmanobrien.com for an immediate interview!
A leading global CRO is offering an exciting opportunity for a Clinical Programmer to join their team. In this role, you will work exclusively with a prestigious global pharmaceutical client that values excellence, rewards achievement, and prioritizes quality. The company fosters an environment of innovation and individuality, welcoming professionals eager to contribute to its dynamic culture. This position is fully remote and open to candidates based in the UK or other locations across Europe.
What you will be doing:
- Provide expertise, delivery and oversight of clinical programming deliverables from study set-up to submission-ready tabulation packages.
- Provide specifications for data models to be used for quality review and for final data model (SDTM); design mapping algorithms for non-standard conversions.
- Ensure quality review of datasets (e.g. Pinnacle 21 compliance checking); ensuring datasets are available for stakeholder use (medical review, central monitoring, adaptive designs) and compliance for database lock.
- Program, or oversee, quality review checks and reports for use by Data Managers and other team members.
- Develop and maintain working knowledge and expertise in programming languages utilized in clinical programming (SAS, SQL).
- Create submission-ready SDTM packages for FDA or other regulatory authorities.
- Acquire and maintain working knowledge in data collection tools such as Medidata Rave, LSAF, Pinnacle 21.
- Work to CDISC standards such as SDTM, CDASH, Controlled Terminology and define.xml.
You will need to have:
- Technically capable, a strong communicator, highly organized and have strong project management skills.
- Bachelors Degree or equivalent in Computer Science, Data Science, Data Engineering, Mathematics or another relevant Scientific field.
- Clinical Programming experience and experience working on a clinical trial.
- Expert knowledge of SAS Programming, Define.xml, SDTM aCRF, cSDRGs.
- Expert knowledge of data structures.
What you’ll receive:
- Generous salary and competitive benefits package.
- Focus on diversity and inclusion plus employee health & wellbeing.
- Fully remote role with excellent work-life balance.
- Immediate interviews available.
Apply now or contact Jo Fornaciari at +44 7488 822 859 / jo@warmanobrien.com for an immediate interview!
Jo Fornaciari
Principal Consultant in Statistical Programming
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