Thermo Fisher Scientific-posted 2 months ago
Full-time • Mid Level
Radnor Township, PA
5,001-10,000 employees

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

  • Act independently as a project lead or lead statistician to deliver the project statistician tasks/responsibilities.
  • Oversee statistical aspects in the design and analysis of laboratory experiments and data.
  • Perform project management functions relating to the administrative and statistical activities of specific project work and team members.
  • Serve as a lead statistician on projects with supervision.
  • Support the development and routine operation of vaccine and biologics assays.
  • Provide statistical support to experimental design, data analysis, assay validation, scientific research and publication, and assay development.
  • Prepare and review reports and protocols.
  • Contribute to the statistical methods section and verify for completeness and consistency.
  • Create SAS programs, graphs, and tables to perform and interpret analyses.
  • Participate in internal meetings.
  • Interact with multiple departments including data management, labs, and IT.
  • Analyze Quality Control data to identify trends or anomalies.
  • Provide training and support to scientists and other non-statistical professionals.
  • Master's degree in statistics, biostatistics, mathematics or related field.
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years).
  • Solid SAS programming experience is required.
  • 1 year of professional work experience within a Lab or working with Clinical Trials is required.
  • Project lead experience is required.
  • MS Office proficiency is preferred.
  • R programming skills.
  • JMP skills.
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