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Warman O'Brien
united kingdom
Senior 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. This is an exciting time to join this inspiring place to work where you will get the chance to ma
Job Source: Warman O'BrienPlanet Pharma
united kingdom
Statistical Programmer - multiple levels Home based #Oncology focused Our client, a global mid-size Pharma, have extended reputation in key therapeutic indications e.g. oncology, rheumatology, rare diseases, etc. and has supported the development of some of the most successful products. Through their particular focus on innovation and a consistent
Job Source: Planet PharmaAIXIAL GROUP
united kingdom
The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, UK, US, Belgium, Czech Republic, Switzerland, Denmark, Romania, and India. The CRO occupies a unique position in the cl
Job Source: AIXIAL GROUPPlanet Pharma
united kingdom
Planet Pharma are partnered with a global Pharmaceutical company who are sitting in the top 10 pharmaceutical companies in the world. We have a few statistical programmer roles within this company at varying seniority levels. The Candidate : Must have experience with SAS and R For higher level someone with submissions experience For Associate Dire
Job Source: Planet PharmaProclinical Staffing
City of London
Job Description Proclinical is seeking a dedicated Principal Statistical Programmer to become part of a global Biostatistics and Programming team. This role is an instrumental part in running and overseeing programming at the study and program level as well as ensuring all work is of the highest quality standards. Responsibilities: - Implement
Job Source: Proclinical StaffingProclinical Staffing
City of London, England, United Kingdom
Proclinical is seeking a dedicated Principal Statistical Programmer to become part of a global Biostatistics and Programming team. This role is an instrumental part in running and overseeing programming at the study and program level as well as ensuring all work is of the highest quality standards. Responsibilities: - Implement effective resource
Job Source: Proclinical StaffingICON Strategic Solutions
united kingdom
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the de
Job Source: ICON Strategic SolutionsTech Observer
united kingdom
Tech Observer is a Global CRO with HO in NJ, USA and presence in other 20+ countries-India, Denmark, UK, Singapore etc. (www.tech-observer.com) We are hiring for following roles on FSP: a. Statistical programmers : 5-8 years of exp in clinical SAS Programming Senior Statistical Programmers : 8-12 years of exp in clinical SAS Programming b. P
Job Source: Tech Observerunited kingdom
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Responsibilities:
Planning, managing and execution of statistical programming deliverables in clinical trial and non-trial activities in the project
Providing input to authority required documents for the trial and non-trial activities
Ensuring that clinical trial and non-trial tasks are aligned with the project specifications
Responsibitly for continuous development of own skills and to contribute to the development of Biostatistics
Providing programming input to the setup of the trial, including but not limited to the CRF, Trial Validation Plan and Data Flow Plan
Ensuring that mock TFLs are created and reviewed by stakeholders
Making AdaM programming according to industry standard and NN specifications
Ensuring that programming, also by co-workers and functional suppliers, is done according to specifications
Ensuring that the inspection readiness documentation is updated at all time during the trial life cycle
Required skills and experience:
5+ years' experience of statistical programming in clinical research or pharma
Extensive experience with programming in e.g. SAS or R
Experience of leading programming activities in clinical trial
Experience with reporting clinical trials, including statistical data handling, analysis and reporting
Experience with review and documentation of programs
Good knowledge of drug development
Experience with clinical database technologies, data models and advanced programming
Experience with collaboration across professional and regional borders
Regular experience with communication and presentations
In-depth knowledge of computer systems and IT
Good knowledge of GxP and guidelines within drug development
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Email Alert for Senior Statistical Programmer jobs in united kingdom
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