A rapidly growing CRO is looking to place a Sr. biostatistician role that is primarily responsible for design, analysis, and reporting of clinical trial data. The role will include working closely with all third-party vendors, in addition to working with in house departments including clinical affairs and data management groups.
The Sr. Biostatistician will be responsible for:
- Utilizing appropriate statistical methodologies to identify and preform clinical trial objectives
- Organizing and overseeing all third-party vendors in order to make sure deadlines are in accordance
- Completing sample size estimations for clinical trials
- Staying current with vital scientific and statistical issues
- Creating statistical models and sampling plans in efforts to aid in product release specifications
- Responsible for answering queries having to do with study design and interpretations from clinical monitors, FDA, or other investigators
The Sr. Biostatistician should have the following qualifications:
- 5+ years of biostatistics in life sciences or a Ph.D. within statistics or other related fields
- Sound understanding of managing complex statistical data and analytic statistical software
- Experience with SAS programming, R coding, and/or SQL
- Understanding of analyzing clinical trial data is a necessity
- Exceptional verbal and written skills
Benefits:
- Various coaching and development opportunities
- Competitive Health plan, FSA, DCA, 401K, Bonus, Vacation and Sick time options
- Emphasized work - life balance including gym memberships, free lunch and snacks, employee discounts, and company social events to list a few
If you are interested in the Sr. Biostatistician role, then please don't wait to apply.
