Principal Biostatistician

This is a fully remote position, open to applicants in United States.

📋 Description

• Independently lead statistical activities for designated Clinical Trials (Phases 1 to 2), from protocol design through to result reporting.

• Act as the Statistics representative on cross-functional trial teams (and potentially indication/project teams), collaborating effectively with all stakeholders.

• Oversee internal programming tasks and/or contributions from CROs for the assigned clinical trials and related activities.

• Contribute to or take the lead on various activities from a statistical viewpoint as necessary, including but not limited to Safety Reporting, ISS/ISE, addressing inquiries from Health Authorities, and Publications.

• Utilize SAS and/or R for tasks such as quality control of datasets and deliverables, inferential statistical analyses, modeling/simulation, and exploratory analyses.

• Engage in and contribute to other initiatives at Cytel or the sponsor side as appropriate.

• Provide oversight to junior Statisticians as needed.

⛳️ Requirements

• A minimum of a Bachelor's degree in statistics or a related field.

• At least 9 years of experience supporting clinical trials in the Pharmaceutical or Biotechnology sector.

• Proven ability to work independently, demonstrating initiative and flexibility through effective and innovative leadership.

• Strong attention to detail and a quality-focused mindset, along with excellent interpersonal and communication skills, fostering innovative and collaborative behaviors.

• Proficient in SAS programming for quality control of critical outputs, efficacy/safety tables, and close collaboration with Programmers.

• Familiarity with R programming (including R Shiny and Python).

🏝️ Benefits

• Ongoing training, development, and support.

• Opportunity to make meaningful contributions to clinical trials.

• Experience working in innovative environments.