Associate Director, Biostatistics

Alnylam Pharmaceuticals; Maidenhead; Hybrid; GBP 90,000 - 120,000; Full time

Job summary

Alnylam Pharmaceuticals in Maidenhead seeks an Associate Director, Biostatistics to lead statistical activities for late-stage clinical trials. You will contribute to trial design, author statistical sections of protocols, and oversee analysis plans, ensuring regulatory standards are met.

The role requires a Ph.D. or equivalent with extensive pharma biostatistics experience, strong communication, and expertise in SAS, R, and CDISC.

Qualifications

• Ph.D. or equivalent with 7+ years pharma biostatistics experience; or MS with 10+ years.
• Excellent written and oral communication and presentation skills.
• Experience programming in SAS and familiarity with CDISC standards.

Responsibilities

• Represent biostatistics in cross-functional team meetings to drive development.
• Collaborate with Clinical Development and Regulatory to design trials.
• Write statistical sections of protocols and oversee analysis plans.
• Contribute to statistical analysis plans and eCRF design.
• Guide CROs and internal teams on statistical conduct of trials.
• Prepare study reports and regulatory documents as needed.
• Support scientific communications and publication activities.

Skills

Leadership

Communication

Cross-functional collaboration

Pharma biostatistics experience

Education

PhD in Biostatistics or Statistics

MS in Biostatistics or Statistics

Tools

SAS

R

EAST

CDISC (SDTM/ADaM/CDASH)

Job description

The Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.

This is a hybrid position, based two days a week onsite at our offices in Maidenhead.

Summary Of Key Responsibilities

• Represents biostatistics at cross-functional team meetings to drive clinical development of drug candidate and provides input on clinical development plans.
• Collaborates with Clinical Development, Regulatory and Clinical Operations Expertise Areas to design clinical trials.
• Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.
• Contributes to or prepares statistical analysis plans.
• Collaborates with Data Management, Clinical Development and Clinical Operations on design of eCRFs.
• Provides statistical guidance on conduct of ongoing trials.
• Collaborates with Statistical Programmers on summary and analysis of trial data.
• Writes ADS and ad hoc analysis specifications.
• Contributes to clinical study reports and other regulatory documents e.g. DSURs, Briefing Documents, etc.
• Represents Alnylam in meetings with regulators, Key Opinion Leaders, partners, and
• other stakeholders
• Contributes to scientific articles, summarizing data collected in Alnylam trials.
• Participates in other activities and meetings to support Biostatistics and the
• Development Team as needed.
• Consults with Research & Preclinical colleagues on statistical questions in their work.
• Manages CRO statistical and programming support.

Qualifications

• Ph.D. in Biostatistics or Statistics or Equivalent with at least 7 years pharmaceutical biostatistics experience; or MS with at least 10 years relevant experience.
• Excellent written and oral communication and presentation skills.
• Experience programming in SAS.
• Interest in and basic understanding of biology and biological processes, including RNAi.

Desired Experience

• Experience in clinical development through Phase 3 (NDA submission).
• Experience as lead statistician for a compound
• Understanding of ICH GCP as well as general knowledge of industry practices and standards.
• Proficiency in R programming language and other statistical software, including EAST.
• Experience with CDISC, including SDTM, ADaM, CDASH.
• Experience in representing sponsors in meetings with interaction with US FDA and international regulatory authorities.
• Experience designing and conducting adaptive trials.