CLINICAL STATISTICAL ANALYST

LOCATION: CORK, IRELAND

REQUIREMENT: EU/UK PASSPORT or IRISH STAMP 4

The purpose of the Clinical Statistical Analyst is to assist during the development of data analysis plans in collaboration with statistical colleagues, physicians, clinical research scientists, and/or medical colleagues. The Clinical Statistical Analyst is responsible for establishing a reporting database and analyzing clinical trial data by working with clinical research associates/clinical data associates and project statisticians.

Statistical Trial Analysis:

· 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.

· Collaborate with other statistical colleagues to write reports and communicate results.

· Be responsible for assisting 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

· Understand relevant disease states and competitive landscapes in order to enhance the level of customer focus and collaboration.

· Ensure replication of tools and systems, where applicable, and stay informed of technology advances.

· Perform work in full compliance with assigned curriculum(s) and be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes and training.

Minimum Qualification Requirements:

· M.S., Ph.D., or equivalent experience

· Statistics, Biostatistics, Computer Science field study or equivalent

Other Information/Additional Preferences:

· Proficiency in a statistical programming language

· 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