Apr
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Remote, 12-month contract with potential to extend long term
This position is to serve as a lead statistician for oncology studies, and to coordinate activities with other functional groups to ensure timely deliverables.
Responsibilities:
Provide statistical expertise for design, analysis and reporting of clinical or pre-clinical studies
Collaborate with various functions on study design and planning, protocol development, statistical methodology and analysis.
Develop statistical analysis plans and analysis specifications.
Collaborate with statistical programming to ensure that analysis is conducted per statistical plan and specifications.
Collaborate with data management and clinical operations to ensure robust CRF and database development and quality data collection.
Collaborate in publications, assist in data interpretation, and ensure consistency and accuracy in data presentation
Contribute to the development of functional-level standards, SOPs, and templates.
Represent biostatistics on study/project teams.
Education, Experience and Skills Requirement:
Ph.D. or M.S. in statistics, biostatistics, epidemiology or related field, work experience as biostatistician in the biotech/pharmaceutical industry or medical research with a minimum of 3 years of experience.
Experience with Phase I & II Oncology trials experience
Ability to work independently and within a team.
Excellent verbal and written communication skills
Good interpersonal and project management skills are essential.
Proficiency in SAS and/or R.
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This position is to serve as a lead statistician for oncology studies, and to coordinate activities with other functional groups to ensure timely deliverables.
Responsibilities:
Provide statistical expertise for design, analysis and reporting of clinical or pre-clinical studies
Collaborate with various functions on study design and planning, protocol development, statistical methodology and analysis.
Develop statistical analysis plans and analysis specifications.
Collaborate with statistical programming to ensure that analysis is conducted per statistical plan and specifications.
Collaborate with data management and clinical operations to ensure robust CRF and database development and quality data collection.
Collaborate in publications, assist in data interpretation, and ensure consistency and accuracy in data presentation
Contribute to the development of functional-level standards, SOPs, and templates.
Represent biostatistics on study/project teams.
Education, Experience and Skills Requirement:
Ph.D. or M.S. in statistics, biostatistics, epidemiology or related field, work experience as biostatistician in the biotech/pharmaceutical industry or medical research with a minimum of 3 years of experience.
Experience with Phase I & II Oncology trials experience
Ability to work independently and within a team.
Excellent verbal and written communication skills
Good interpersonal and project management skills are essential.
Proficiency in SAS and/or R.
#J-18808-Ljbffr