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Senior Statistician II

Role overview

Qualifications

  • Experience in statistical analyses and programming
  • Strong leadership and project management skills
  • Proficiency in writing protocols and analysis plans
  • Ability to mentor and guide team members

Responsibilities

  • Ensure compliance with departmental SOPs and contribute changes as needed
  • Lead and manage complex projects and team members
  • Review and contribute to statistical analysis protocol and documentation
  • Prepare reports and contribute to Integrated Clinical and Statistical Reports

Key facts

Hard skills

Other skills

  • Plan Execution
  • Report Writing
  • Mentorship
  • Communication
  • Teamwork

About the company

Thermo Fisher Scientific logo

Thermo Fisher Scientific

  • Biotech & Genomics
  • 10,001+
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.

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Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

• Ensures compliance with the activities outlined in the department's SOPs and 
contribute changes as needed. Follows departmental procedures for statistical 
analyses and programming work. 
• Work independently as a project lead or as lead statistician to deliver on lead 
tasks/responsibilities across challenging projects; provides senior review on 
projects. Leads team members across multiple complex projects. Interacts with 
the sponsor on all aspects of the project and present to sponsor and regulatory 
agencies as needed. 
• Reviews sample size calculations and protocols for completeness, 
appropriateness of clinical design, and sound statistical analysis. Contributes to 
writing appropriate protocol sections. Reviews randomization related 
documentation.
• Writes / reviews analysis plans and guide others on the team in its 
implementation. Defines appropriate methods and procedures for statistical 
analysis. Reviews statistical analysis for key efficacy endpoints.
• Reviews specifications for analysis database, oversees its development, and 
assures completeness for use in all programming. Oversees collaboration with 
programmers and data management personnel as to database maintenance, 
updating, and documentation. Supervises creation of table and listing 
specifications. 
• Prepares reports, manuscripts, and other documents. Contributes statistical 
methods section for Integrated Clinical and Statistical Report, Integrated 
Summaries of Safety, Integrated Summaries of Efficacy, and other documents. 
• Monitors project budget as it relates to project work scope and communicate 
proactively with management concerning potential changes in work scope. 
Communicates with sponsors concerning project work scope and budgetary 
changes after reviewing with management. 
• Mentors members of the department by providing project guidance and 
statistical advice and by promoting employee development, contributing to 
performance planning, and providing resource planning. 
• Provides input on hiring recommendations, department policies, and resourcing 
requirements. 
• Acts as representative of the department to other divisions. Assists in bidding 
and business development activities. Consults with business development with 
respect to bids and timelines.

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