Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life cycle in accordance with project, organizational and regulatory standards. Act as subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Participate in the promotion of the employer as a global research organization, by contributing to the development, publishing, and reporting of project data.
Responsibilities
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Analysis Services: Carry out statistical analyses and provide direction to programmers, using standard
software packages to interpret and translate results.
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Academic Research Support: Convert and present biometrical trial technologies, processes and findings into publishable and promotable scientific processes and results.
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Project Support: Provide statistical expertise and guidance based on established methodologies
throughout the project life cycle.
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Statistical Analysis/Data Collection Planning: Prepare statistical analysis plan and oversee project data collection, management, and analysis with input from the project teams.
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Study Report Support: Assist medical director(s) and/or technical writers by preparing statistical section of
study report, publications and/or presentations.
Qualifications
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Upper Intermediate communication skills in English, both written and oral
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Post-graduate degree/ professional designation (ie. CPA, PEng, MD) and 1-3 years’ related experience with initial and On-going training.
OR
Post-graduate degree or undergraduate degree with professional certification(s) Level and 4-6 years related experience +substantial on-going job related training
Who can apply?
You can apply if:
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