• Join our Clinical Research team as a Principal Scientist in Biostatistics • Contribute to advancing life-changing therapies through statistical excellence • Work closely with clients while utilizing the benefits and resources of Thermo Fisher Scientific • Responsible for implementing diverse statistical tasks throughout the full clinical trial process, from study design and protocol writing to final analysis and reporting • Opportunity to impact health outcomes while working with advanced clinical development programs

• The Lead Biostatistician functions independently as a project lead or lead statistician to deliver the project tasks/responsibilities. • Performs project management functions relating to the administrative and scientific activities of specific project work and team members. • Oversees statistical aspects in the design and analysis of clinical trials, including project management, statistical analysis, report preparation, and advising other project statisticians. • Supports the department by directly contributing to simple or moderately complex study protocols and bid defenses, including organizing teams and implementing strategies to ensure process and programming efficiencies.

• Providing statistical support to clinical studies • Participating in the development of study protocols, including participation in study design discussions and sample size calculations • Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications • Performing statistical analyses and interpreting statistical results • Preparing clinical study reports, including integrated summaries for submissions • Utilizing your strong communication skills to present and explain the methodology and consequences of decisions • Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions. • Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros • Participate in the development of CRFs, edit check specifications, and data validation plans • Provide review and/or author data transfer specifications for external vendor data • Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals • Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices

We are looking for an experienced Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support or lead one or more Phase I-IV clinical studies. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same. Sponsor-dedicated Working fully embedded within one of our pharmaceutical clients, you'll be at the heart of our client's innovation. As a Senior Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview Our Senior Biostatisticians perform statistical analyses to support clinical trial/marketed product submissions to regulatory agencies. Having exposure to Oncology is a bonus. Responsibilities As a Senior Biostatistician, your responsibilities will include: - Providing statistical support to clinical studies - Participating in the development of study protocols, including participation in study design discussions and sample size calculations - Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications - Performing statistical analyses and interpreting statistical results - Preparing clinical study reports, including integrated summaries for submissions - Utilizing your strong communication skills to present and explain the methodology and consequences of decisions - Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions. - Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros - Participate in the development of CRFs, edit check specifications, and data validation plans - Provide review and/or author data transfer specifications for external vendor data - Collaborate with internal and external functions (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals - Provide review and/or author SOPs and/or Work Instructions related to statistical programming practices