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Biostatistician V Jobs
Company | Fred Hutch |
Address | Seattle, WA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Research Services |
Expires | 2023-09-19 |
Posted at | 9 months ago |
Overview
- Perform other responsibilities as required.
- Maintain functional understanding of standard policies and procedures and complete required training in a timely manner; Contribute to the development and maintenance of standard procedures and related quality documents.
- Generate written summaries for use in customized statistical lab reports.
- Participate in and lead internal project initiatives which may include developing new tools and processes, evaluating new statistical software packages, or exploring other value-added team activities.
- Collaborate with PhD statisticians/epidemiologists, Statistical Research Associates (SRAs), laboratory scientists, laboratory data managers, and other subject-matter experts to provide statistical support for clinical studies and research projects or laboratory data and analyses including statistical considerations and planning (power and sample size calculations), randomization lists, consultation, study data analyses, and written summaries and tables of results for use in study reports - for example, Dataand Safety Monitoring Boards or other interim review meetings, scientific abstracts and manuscripts, and/or tables in support of a Clinical Study Report for submission.
- Represent SCHARP and the data analytics unit at professional meetings.
- Participate in and lead verification of standard reports prepared by programmers or other team members.
- Contribute to and review study documents including protocol drafts, statistical analysis plans, case report forms, and other documents as required.
- Mentor or formally supervise more junior SRAs as required. Conduct performance reviews of direct reports.
- Participate in and lead when appropriate protocol team conference calls and meetings, organizational meetings, interim data review meetings, scientific meetings, regional meetings and internal team meetings as required.
- Apply and adhere to CDISC data standards and guidelines where required in the production of analysis datasets and reports; assist in the production of supporting CDISC documentation for submissions (Define.xml, Reviewer’s Guides).
- Collaborate with data management and operations in the development of quality assurance procedures for on-going data collection, cleaning and analysis - such as establishing edit checks, or HIVendpoint verification.
- A minimum of 5 years of related work experience is required.
- Thorough understanding of GCP and regulatory requirements.
- Strong oral and written communication skills.
- High-level proficiency with SAS or R (as required by specific team/project).
- MS or PhD degree in Statistics or Biostatistics or related field with demonstrated work experience.
- Minimum of 2 years of experience statistical project management.
- Demonstrated functional knowledge of general statistical practice within clinical trials.
- Thorough understanding of statistical programming process and best practices.
- Proven track record of collaboration with internal and external partners.
- Minimum of 2 years of experience in a senior, lead or management role.
- Strong organizational and multi-tasking skills.
- High functional knowledge of statistical practice within network specialization.
- Experience with laboratory assay data.
- 3+ years of experience in statistical project management.
- Able to lead and advise on network-specific statistical tasks.
- Thorough understanding of network needs and objectives.
- 3+ years of experience in a senior, lead or management role.
- 7+ years of relevant work experience.
- Experience with R-markdown.
- VISC-specific preferences
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