
Senior Biostatistician (FSP)
- Durham, NC
- Permanent
- Full-time
- Home-based remote working opportunities
- Work/life balance as well as flexible schedules
- Collaborating with dedicated, high-performance, statistical and research teams
- Variety of therapeutic areas, indications and, study phases
- Technical training and tailored development curriculum
- Research opportunities that match your unique skillset
- Promising career trajectory
- Job stability: long-term engagements and re-deployment opportunities
- Focus on bringing new therapies to market rather than project budgets and change orders.
- Validate Statistical outputs and datasets.
- Interact with members of the multidisciplinary project teams to establish project timelines.
- Provide statistical input to study protocols.
- Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.
- Write statistical analysis plans.
- Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
- Collaborates with Data Management, Clinical Development, and Clinical Operations on design of eCRFs.
- Contributes to clinical study reports and other regulatory documents e.g., DSURs, Briefing Documents, etc.
- Provide guidance and supervision to programmers in authoring of analysis dataset specifications and programming of tables, listings, and figures.
- Interpret study results and review reports of study results for accuracy.
- Participate and contribute to authoring of Clinical Development Plan.
- Support exploratory analyses and medical affairs publications.
- Participate in pre-IND and NDA activities.
- Participate in the development and enforcement of SOPs and guideline.
- Participates in other activities and meetings to support Biostatistics and the Development Team as needed.
- Consults with Research & Preclinical colleagues on statistical questions in their work.
- PhD in Statistics, Biostatistics, or related field with 3+ years industry experience.
- MS in Statistics, Biostatistics, or related field with 5+ years of industry experience.
- 1+ years with regulatory submissions
- Successful publication experience.
- Demonstrate ability to work independently in project management and decision making.
- Able to effectively communicate his/her ideas and to manage programmers in a constructive manner.
- Ability to use SAS and/or R to perform efficacy analyses and validate important data derivations when necessary.
- Experience with simulations.
- Understanding of ICH GCP as well as general knowledge of industry practices and standards.
- Familiarity with R programming language and other statistical software, including EAST.
- Experience with Neuroscience therapeutic area.
- Experience with CDISC, including SDTM, ADaM, CDASH.
- Experience with Multiple imputations.
- Knowledge of simulations, multivariate analyses, and biomarker analyses