Biostatistics Associate Director (HYBRID)

Vertex Pharmaceuticals; Boston (MA); On-site; USD 174,800 - 262,200; Full time

Benefits offered by this job

Annual bonus

Generous paid time off

Educational assistance programs

Commuting subsidy

401(k) matching

Company equity awards

Job summary

Vertex Pharmaceuticals in Boston is seeking a Biostatistics Associate Director to lead statistical analyses for clinical trials. The role requires a Ph.D. in Statistics, 7+ years of relevant experience, and proficiency in SAS and R.

The successful candidate will manage biostatistics projects, author Statistical Analysis Plans, and collaborate with cross-functional teams to ensure quality outcomes. Benefits include hybrid work options, competitive salary, and generous paid time off.

Qualifications

• Typically requires 7 years of experience with a Ph.D. or equivalent education.
• Experience with NDA/MAA and interactions with USA/European regulators is preferred.

Responsibilities

• Conducts all statistical work for clinical trials and observational studies.
• Leads biostatistics projects, including work allocation and presentation to review boards.
• Authors Statistical Analysis Plans and develops data review plans.
• Collaborates with statistical programming to ensure timely delivery and quality.

Skills

SAS

R statistical software

Advanced statistical methods

Critical thinking

Excellent written communication

Team collaboration

Education

Ph.D. in Statistics or Biostatistics

Job description

## Biostatistics Associate Director (HYBRID)Applylocations: Boston, MAtime type: Full timeposted on: Posted Todayjob requisition id: REQ-29452**Job Description****General Summary:**Biostatistics Associate Director will perform sophisticated scientific statistical analyses in support of the company's Global Medicines Development and Affairs area with minimal guidance and mentoring on new and complex issues. The incumbent will completed work in a resourceful, self-sufficient manner and create alternative approaches to achieve desired results. The incumbent is capable of independent strategic and technical contributions. The incumbent should possess a good knowledge of related disciplines while performing Biostatistics activities with a drug developer mindset.**Key Duties and Responsibilities:*** Conducts all scientific and operational statistical work for multiple clinical trials, observational studies, or real world data (RWD) investigations.* Leads biostatistics projects or major components of a project including work allocation and review.* May include presentation to the Peer Protocol Review Committee (PPRC) or other internal senior review boards.* Possesses an advanced and in-depth understanding of modern drug discovery and development processes.* Represents Biostatistics as a member of cross functional teams, providing input and specialized technical guidance to elicit meaningful and/or productive outcomes.* Authors study Statistical Analysis Plans (SAPs), including table, figure, and listing (TFL) shells. Develops Cross-functional Data Review (xFDR) plan, Key Reports Memo (KRM), and Data Dissemination Plan (DDP) in order to facilitate the review, summary, and dissemination of key study data/results.* Collaborates with statistical programming and other functions to ensure timely delivery of TFLs with high quality.* Contributes to clinical study reports (CSRs) and related processes, authoring or co-authoring methodological or study-related publications and posters.* Provides input into programming specifications and review.* Contributes to external interactions with regulators, payers, review boards, etc.* Authors or co-authors methodological or study-related publications and posters.* Determines and implements design and analysis methods at the study or project level and participates in Statistical Review Forum (SRF) discussions of studies assigned to others.* Contributes to departmental working group efforts on various advanced technical and operational issues.* Independently undertakes new and complex issues.* Completes assigned work in a resourceful, self-sufficient manner, often conceptualizing alternative approaches to achieve desired results.* Develops breadth of knowledge across related disciplines with a drug developer mindset.**Knowledge and Skills:*** Some prior staff management experience is typical* In-depth competence with SAS and R statistical software* In-depth understanding of advanced statistical methods used in drug development* Ability to show critical thinking with logical problem-solving* Excellent written and verbal communication skills* Excels in a team environment* Collaborates well with non-statisticians* NDA/MAA experience and direct dealings with USA/European regulators**Education and Experience:*** Ph. D. in Statistics or Biostatistics.* Typically requires 7 years of experience with a Ph.D. or the equivalent combination of education and experience.**Pay Range:**$174,800 - $262,200**Disclosure Statement:**The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.**Flex Designation:**Hybrid-Eligible Or On-Site Eligible**Flex Eligibility Status:**In this Hybrid-Eligible role, you can choose to be designated as: 1. **Hybrid**: work remotely up to two days per week; **or select** 2. **On-Site**: work five days per week on-site with ad hoc flexibility.Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.