Alnylam Pharmaceuticals

Associate Director, Biostatistics

Alnylam Pharmaceuticals$218K — $250K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Biostatistics, Statistics, Mathematics, Biology or related field.
  • 7+ years of experience in biostatistics or related occupation.
  • Proficient in SAS programming and R programming language.
  • Experience with Bayesian analysis and dose-response modeling.
  • Knowledge of clinical development processes through Phase 3 and ICH GCP standards.
  • Familiarity with CDISC standards (SDTM, ADaM, CDASH).
  • Proven ability to represent organizations in discussions with US FDA and international regulatory bodies.

Responsibilities

  • Represent biostatistics at cross-functional team meetings for drug development.
  • Collaborate with various teams to design clinical trials and provide statistical input.
  • Write statistical sections for clinical trial protocols and consult with experts.
  • Prepare statistical analysis plans and support ongoing trials with statistical guidance.
  • Work with Data Management on electronic CRFs design.
  • Collaborate with Statistical Programmers on trial data analysis.
  • Contribute to clinical study reports and regulatory documentation.

Benefits

  • 100% telecommuting role allowing for flexible work from anywhere.
  • Opportunity to collaborate with top-tier experts and regulatory authorities.
  • Involvement in significant clinical development projects through Phase 3.
  • Engagement in scientific publication efforts to disseminate trial data.
  • Support for continued professional development and statistical consulting.
Full Job Description
JOB TITLE: Associate Director, Biostatistics JOB DUTIES: 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. 100% telecommuting role. Reports to company headquarters in Cambridge, MA. Can work remotely or telecommute. MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS: PhD degree in Biostatistics, Statistics, Mathematics, Biology or related field of study and seven (7) years of experience in the job offered or related occupation in which the required experience was gained. Must have demonstrated experience with: SAS programming; Bayesian analysis; dose-response modeling; superiority and futility interim analysis; clinical development through Phase 3; ICH GCP; R programming language and statistical software (EAST); CDISC (SDTM, ADaM and CDASH); representing sponsors in meetings with interaction with US FDA and international regulatory authorities; and designing and conducting adaptive trials. OTHER: Employer: Alnylam US, Inc. Job location: 675 W Kendall Street, Cambridge, MA 02142. 100% telecommuting role. Reports to company headquarters in Cambridge, MA. Can work remotely or telecommute. 40 hours/week; $218,540.25.00 - $250,700.00/Year (view contact information below) If offered employment, must have legal right to work in U.S.

About Alnylam Pharmaceuticals

Alnylam Pharmaceuticals is a biotechnology company that focuses on RNA interference (RNAi) therapeutics. The company's products are designed to silence specific genes that cause diseases. Alnylam's pipeline includes products for the treatment of genetic, cardio-metabolic, and hepatic infectious diseases. The company was founded in 2002 and is headquartered in Cambridge, Massachusetts.
Learn more about Alnylam Pharmaceuticals
Size
1,665 employees
Market Cap
$28.7 billion
Industry
Net Income
-$858.2 million
Founded
2002
5 Year Trend
+78.1%
Revenue
$492.8 million
NASDAQ

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