Associate Director, Biostatistics

Alnylam Pharmaceuticals

3d•$185,300 - $250,700

About The Position

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 role represents biostatistics at cross-functional team meetings to drive clinical development of drug candidates and provides input on clinical development plans. The Associate Director collaborates with Clinical Development, Regulatory, and Clinical Operations Expertise Areas to design clinical trials, writes the statistical sections of clinical trial protocols, and contributes to or prepares statistical analysis plans. They also collaborate with Data Management, Clinical Development, and Clinical Operations on the design of eCRFs, provide statistical guidance on the conduct of ongoing trials, and collaborate with Statistical Programmers on the summary and analysis of trial data. Additionally, this role involves writing ADS and ad hoc analysis specifications, contributing to clinical study reports and other regulatory documents (e.g., DSURs, Briefing Documents), and representing Alnylam in meetings with regulators, Key Opinion Leaders, partners, and other stakeholders. The Associate Director also contributes to scientific articles, participates in other activities and meetings to support Biostatistics and the Development Team, and consults with Research & Preclinical colleagues on statistical questions. A key responsibility includes managing CRO statistical and programming support.

Requirements

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.

Nice To Haves

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.

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.