Senior Biostatistician

Ockham is a global provider of resources to the Biotechnology and Pharmaceutical Industry. We work with companies involved with clinical trials and other market approval processes to help them deliver their products on time and on budget.  One of our clients in Seattle, WA has an immediate need for a Senior Biostatistician. This is a contract position.

1.      Be responsible for all statistical tasks on the assigned clinical trials, and perform these tasks with a high level of independence.  Examples of these tasks include clinical trial design/planning, statistical analysis plan, data interpretation/reporting, exploratory analyses and additional analyses to support publications, and statistical consultation throughout the lifetime of the clinical trial

2.      Tracking clinical trial activities and milestones.

3.      Collaborate with SAS programmers to ensure timelines are met and to ensure adequate quality of all Biostatistics deliverables for the assigned trials.

4.      Follow CTI SOPs, TGIs, as well as Health Authority requirements (e.g., GCP, regulatory guidelines).

5.      Establish and maintain sound working relationships and effective communication with the clinical study team.

6.      Participate in non-clinical projects (initiatives, process teams etc.) as needed

Requirements include:

·       M.S. in Biostatistics/Statistics with a minimum of 5 years of related experience, or

·       PhD in Biostatistics/Statistics with a minimum 2 years of related experience

Preferred experience includes:

• Directing SAS programmers,
• Regulatory filing experience,
• Experience with oncology clinical trials.