Description
For this role we are looking for experienced Biostatisticians with several years of experience related to clinical research in the pharmaceutical or medical device industry. The candidate should be able to lead and coordinate a team of statisticians and programmers working on multiple projects. Excellent communication skills will be required with an ability to clearly explain statistical concepts to a large audience consisting of other non statistical peers, scientists and non-scientist.- Provide input on internal projects with regard to protocol development, sample size, data collection, and reporting.
- Provide statistical plans for studies and tables for reports, publications and presentations
- Be accountable for the biostatistical aspects of the assigned Clinical Studies. Bring biostatistical input where needed in all study related documents (e.g., Study Protocols, Statistical Analysis Plans, Study Reports, publications, presentations)
- Apply biostatistical principles, techniques and practices to develop the methodology to assess development products.
- Guide and monitor the selection of appropriate statistical methods for the design and data analysis of clinical studies.
Experience:
- Masters in Statistics or related field, 5+ years experience with clinical trials in the medical device, biotech, or related industry.
- Ph.D. in Statistics or related field preferred.
- Higher proficiency in SAS programming essential and R desirable.
To find out more about Real please visit www.realstaffing.com