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Senior / Principal Statistical Programmer
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Proclinical are recruiting for a Senior / Principal Statistical Programmer to work at a leading multinational contract research organisation in Spain. This is an excellent company to work for, whose clients include many of the world's leading pharmaceutical and medical device companies and they employ over 15,000 personnel in over 50 countries.
Job Responsibilities:
- Provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data.
- In addition, the Senior Statistical Programmer can fill the Statistical Programming Coordinator role on projects, and liaise with sponsors, Data Operations Leads, and other functional areas as required.
- General areas of responsibility also include: import/export programming specification development, test data creation and test data entry, import/export programming functional testing, as well as mapping specifications to support relevant data standards.
- Recognized as a subject matter expert, will provide technical support and expert advice to internal and external sponsors.
- In addition, the Principal Statistical Programmer can fill the Statistical Programming Coordinator role on projects, liaise with sponsors, Data Operations Leads, and other functional areas as required.
- Further, the Principal Statistical Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets.
- General areas of responsibility also include: import/export programming specification development, test data creation and test data entry, import/export programming functional testing, as well as mapping specifications to support relevant data standards.
Skills and Requirements:
- Proficiency in SAS.
- Knowledge of the programming and reporting process.
- Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
- Demonstrated application of CRS concepts to achieve best practice and promote continuous improvement.
- Demonstrate ability to learn new systems and function in an evolving technical environment
- Strong leadership ability.
- Ability to successfully work together with a ("virtual") team (including international teams as required) as well as independently.
- Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change.
- Attention to detail.
- Excellent analytical skills.
- Good presentation skills.
- Tenacity to work in an innovative environment.
- Ability to negotiate and influence in order to achieve results.
- Business/Operational skills that include customer focus, commitment to quality management and problem solving.
- Good business awareness/business development skills (including financial awareness)
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Sonia Buxeda Mas on +34 911 231 297 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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