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Details
Clinical Statistical Analyst
Reference: | SCA014044 | Location: |
Cork |
Qualification: | Degree | Experience: | 4-5 Years |
Job Type: | Permanent | Salary: | Not Disclosed |
May be suitable for:
Biostatistician, SAS programmer
Clinical Statistics Analyst
Our client, a global pharma company, are continuing to grow their Statistics team and are currently recruiting for a Clinical Statistics Analyst to join their team on a permanent basis. As Clinical Statistical Analyst, in collaboration with statistical colleagues, physicians, clinical research scientists, and/or medical colleagues you will assist during the development of data analysis plans. You will be responsible for establishing a reporting database and analyzing clinical trial data by working with clinical research associates/clinical data associates and project statisticians.
Responsibilities:
- Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans
- Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, creating the reporting database, and conducting the actual analysis once a reporting database is created
- Collaborate with data sciences in the planning and implementation of data quality assurance plans
- Effectively justify methods selected and implement previously outlined analysis plans
- Conduct peer-review of work products from statistical colleagues
- Maintain proficiency with respect to statistical programming and statistical methodology and in applying new and varied methods
- Maintain current knowledge of CDISC data standards
- Effectively utilize current technologies and available tools for conducting the clinical trial analysis
- Communication of Results and Inferences
- Collaborate with other statistical colleagues to write reports and communicate results
- Assist in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers
- Assist or respond to regulatory queries working in collaboration with other statistical colleagues
- M.S., Ph.D., or equivalent experience
- Statistics, Biostatistics, Computer Science
- 5+ years of relevant experience that includes 3 major pharma
- Experience in all major phases of drug development that includes immunology
- Regulatory response experience that is an asset
- High level of expertise in programming that is a huge plus for a project statistician
- Proficiency in a statistical programming language(s)
- Interpersonal/teamwork skills for effective interactions
- Technical growth and application with working knowledge of statistics and statistical software
- Self-management skills with a focus on results for timely and accurate completion of competing deliverables
- Creativity and innovation
- Demonstrated problem solving ability and attention to detail
- Data analysis, technology, and systems expertise
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
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