Biostatistician II – Early Development Studies
Posted 29 days ago
You'll complete your application on Thermo Fisher Scientific's career site.
About the Role
This mid-level biostatistician position serves as an autonomous project lead tasked with managing essential statistical deliverables for global research initiatives. You will support the progression of early-stage clinical trials, ensuring rigorous technical quality, strict adherence to project schedules, and the advancement of innovative medical treatments. The role demands an organized, proactive mindset focused on data accuracy. Operating in a cross-functional, international team, you will engage with partners and sponsors to support successful trial operations. Success requires clear communication, the flexibility to navigate changing priorities, and a commitment to scientific rigor, utilizing sophisticated statistical techniques and programming expertise to define analytical strategies.
Requirements
- You must possess a Master's degree in biostatistics, statistics, mathematics, or a closely related discipline.
- At least two years of professional biostatistics experience is necessary, preferably within a Contract Research Organization environment.
- You are required to be proficient in SAS, including specific competency in STAT, BASE, GRAPH, and MACRO, along with a firm understanding of statistical modeling.
- Prior experience using R is viewed as a beneficial qualification.
- You must demonstrate a deep understanding of statistical theory and the ability to author specifications for listings, tables, and figures.
- Strong capabilities in project management and high-level English communication skills are essential to drive collaboration within a diverse, global team.
- You must demonstrate a dedication to complying with safety guidelines and Good Manufacturing Practices.
Responsibilities
- You will act as the primary statistician for specific projects, undertaking intricate statistical evaluations and creating requirements for figures, listings, and tables.
- Your work involves evaluating clinical protocols for their design suitability and thoroughness, performing sample size estimations, and creating randomization processes.
- You will draft statistical analysis plans and utilize SAS software to produce analysis-ready datasets and deploy various models.
- It is your responsibility to verify the precision and consistency of statistical methodologies within manuscripts, reports, and other documentation.
- You will manage coordination with data management teams and programmers to oversee databases, track project spending against the project scope, and serve as the main point of contact for sponsors regarding all statistical components of your assigned work.
Benefits & Perks
- This is a 100% remote job that features flexible scheduling to enable efficient teamwork and participation in meetings across different time zones.
- Adjustable hours are provided during the introductory training and orientation phases to guarantee adequate time to interact with global colleagues.
Note: This listing is summarized and paraphrased by WorkNow from a publicly posted role. For the original wording and full details, please refer to the employer's official posting.
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