Description
We are seeking a Biostatistician to prepare analysis plans and write detailed specifications for analysis files, tables, listings and figures. You will interpret analyses and write statistical sections of study reports, and provide training, guidance and mentorship to lower level and new staff.
Responsibilities:
- Prepare analysis plans and write detailed specifications for analysis files, tables, listings and figures
- Interpret analyses and write statistical sections of study reports
- Provide training, guidance and mentorship to lower level and new staff
- Production of High-Quality Deliverables: Complete and review complex assigned tasks with a focus on accuracy
- Leadership: Perform statistical team lead role on single studies, working closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget
- Data Management: Assist in reviewing or advising data management staff on database design, validation checks and critical data
- Statistical Analysis Plan (SAP) and Shells: Author or perform quality control review of SAPs and shells
- Datasets: Write and maintain programming specifications, program assigned datasets to industry standards
- Tables, Listings and Figures (TLFs): Write programming specifications for statistical analyses outputs, program TLFs, and check resulting output for format and content
- Timelines: Plan and document timelines, forecast resource needs, suggest work may be out of scope
- Financials: Share accountability for the financial success of assigned studies, control costs and maximize revenue recognition
- Knowledge Sharing: Help train staff regarding operational items, mentor junior staff
- Risk Management: Identify risks to project delivery and/or quality, propose solutions to mitigate risks
Requirements:
- Bachelor's Degree in Biostatistics or related field and 1-3 years relevant experience
- Master's Degree in Biostatistics or related field and 1-3 years relevant experience
- Ph.D. in Biostatistics or related field
- Intermediate level knowledge of principles, theories, and concepts of a job area
- Excellent written and oral communication skills, including grammatical/technical writing skills
- Excellent attention and accuracy with details
- In-depth knowledge of applicable clinical research regulatory requirements
- Strong individual initiative, strong organizing skills, strong working knowledge of SAS computing package
- Familiarity with other relevant statistical computing packages such as StatXact
- Strong commitment to quality, ability to effectively manage multiple tasks and projects