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Dear Allstat,
SEC Recruitment is currently recruiting for a number of positions across the UK and mainland Europe. Please find below a further selection of vacancies currently on offer:
1805/12a
FREELANCE: Project Programmer / Lead Statistical (SAS) Programmer
Based in Mainland Europe
£ Excellent Rate / hour – Dependant on Experience
Job Summary:
We are seeking a highly skilled
Project Programmer / Lead Statistical Programmer with expert SAS development knowledge to join a major our pharmaceutical client on an exciting & challenging freelance opportunity.
Provide input as appropriate to all meetings, discussions and activities covering all SAS programming aspects for assigned clinical trials. Programming of analysis datasets, pooled datasets, listings, summaries,
figures and tables for the reporting and analysis of the clinical trials and of the ISS and ISE according to the specifications of the client.
- Excellent SAS programming skills with proven experience in the pharmaceutical industry
- Proven SAS programming experience in the area of analyzing & reporting of clinical data
- Profound knowledge in Statistics, degree in Statistics is a plus (Or Equivalent)
- knowledge in CDISC standards, especially SDTM, ADaM.
Desirable Experience:
Experience in Clinical Project management
Ref: 0512/11a
CONTRACT: SAS Programmer
Based in Souith East, UK
£ Excellent Rate / hour – 6 month rolling
Job Summary:
1. Proven SAS programming experience in pharmaceutical and/or CRO environment
2. Very good SAS programming knowledge (Base SAS, SAS/GRAPH, SAS/STAT, macro programming, reporting, SQL), familiarity with ODS RTF/ HTML
3. A sound understanding of basic statistical principles and the basics of statistical programming
4. Knowledge of the data management process in clinical drug development
5. Good knowledge of medical coding processes, standards and issues
6. Expertise in working with pooled, safety and efficacy data
7. Good analytical skills
8. Excellent interpersonal and team working skills
9. Good communication and presentation skills, both oral and written
10. Knowledge of regulatory requirements, e.g. ICH guidelines for statistical reporting
11. Comprehensive knowledge of clinical and pharmaceutical drug development process and GCP requirements
12. Multiple phase experience in clinical research
13. The ability to work independently and prioritise your own workload
Highly Desirable:
Experience in safety data analysis
Programming skills in any of the following: JavaScript/VBScript, Java, VBA, XML, XSLT, SQL, Microsoft Excel
Exposure to investigational new drug application (IND) annual reports and Development Safety Update Reports (DSURs)
Experience of signal detection in clinical data
0702/12a
FREELANCE: Senior / Lead Statistical Programmer
Based in South East, UK
£Excellent Rate / hour – Dependant on Experience
Job Summary:
Working for this major pharmaceutical company, you will ensure;
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all programming outputs pertaining to individual clinical studies and ISS/ISE meet required standards and are validated / correct
·
all programming outputs pertaining to non-registrational activities meet required standards and are validated and correct
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quality and accuracy of programming deliverables.
·
Assist in the recruitment of programming staff
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Provide support to (mentor) more junior programmers
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Participate in technical programming and process improvement initiatives within Global Biostatistics
·
Function as a Project Lead Programmer with the following key activities
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Set up study level programming environment
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Generate randomization lists
·
Draft SDF dataset specifications
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Review and approve SDF dataset specifications drafted by another programmer
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Review and approve key study-related documents produced by other functions (e.g. CRF, Data Management Plan etc)
·
Review SAPs from the programming perspective
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Draft programming plans
·
Review and approve programming plans drafted by another programmer
·
Write, test and validate software programs to produce SDF and analysis datasets and TLGs for inclusion within CSRs, ISS / ISE, publications and other communications
·
Perform QC checking of software programs written by another programmer
Educated to BS/BSc or higher degree in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific subject your knowledge will encompass;
·
Minimum 5 years' statistical Programming with the pharmaceutical industry
·
Clinical Trials within Pharmaceutical/Biotechnology/Public Health setting in Industry, Government or Academia
·
Drug Development (Pre-clinical Development, Clinical Development, Medical Affairs)
·
Project Planning and Management
·
Development of policies and SOPs
·
International co-operation
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Team working
·
relevant career experience
For a confidential discussion or further information on any of the positions, please feel free to call me on +44(0)207 255 6600 or email an updated CV to
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Best regards,
Priya
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