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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.