A biotech company is actively seeking a new Senior Manager, Biostatistics for a great Remote opportunity with their staff.

Responsibilities:

Contribute to study level tasks from statistics perspective, including study design and sample size determination
Author/review statistics section in the protocol, SAP and DMC charter
Create/review study randomization files; develop TFL shell and specification; review CRFs and other study documentations
Work collaboratively within the Biometrics teams and with cross-functional teams to meet product deliverables and timelines for statistical data analysis and reporting
Ensure statistical integrity of deliverables; provide statistically sound scientific methodology input to meet project objectives and regulatory statistical and data requirements
Independently conduct analyses suggested by the data; Propose new/novel statistical methodological approaches to improve the efficiency and sensitivity of study results
Contribute to developing standards and research in advanced statistical methodologies
Author/review regulatory documents or scientific publications

Qualifications:

PhD in Statistics or Biostatistics with a minimum of 5 years (min 8 years for Master's degree) of post-graduate experience in the Clinical Trials setting in the Pharmaceutical industry
Experienced in NDA / BLA / MAA activities as a key contributor from statistics perspective and direct involvement in regulatory interaction
Experienced as a Study Lead Statistician and contributing to strategy discussion in cross functional settings
Experienced in study level work including authoring SAP and TFL specification
Familiar with ICH guidelines, FDA / EMA / other regulatory authority guidance
Solid understanding of Mathematical and Statistical principles
Detailed-oriented with organization, problem solving and prioritization skills

Desired Skills:

Familiar with SAS and R with knowledge in CDISC including SDTM, ADaM, and controlled terminologies

Remote work,