Job Description
Executive Director, Biostatistics
Job Location:  Bridgewater, New Jersey, USA
Job Requisition ID:  14195

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.

 

 

As we expand our development capabilities, we are seeking an Executive Director, Biostatistics to establish and lead the biostatistics function across the entire portfolio. The Executive Director, Biostatistics is a pivotal leadership role within R&D, positioned to shape global development programs and influence regulatory strategy at the organization level. This position will report to the VP and Head of Development and is also expected to build and expand internal biostatistics team. This individual will serve as a strategic and technical thought partner to collaborate with cross-functional development leaders, including Clinical, Regulatory and Translational Sciences.

 

Responsibilities:

 

  • Serve as the company’s statistical authority and leader, accountable for statistical strategy, oversight, and execution across the full clinical development lifecycle
  • Provide immediate leadership for a high priority newly acquired Phase 3 asset, including study design, data strategy, and statistical oversight
  • Drive statistical leadership for all key programs, including IND-enabling work, multiple phase 2/3 trials, global regulatory submissions, and post-marketing requirements
  • Partner with clinical development leadership on clinical strategy, program risk assessment, and decision making at the highest levels
  • Lead the design, statistical modeling, and analysis planning for clinical trials with appropriate balance of innovation and regulatory rigor
  • Oversee and/or author development of key statistical documents, including Statistical Analysis Plans (SAPs), protocols, and regulatory components of global regulatory submissions
  • Oversee internal biostatistical resources and lead strategic outsourcing to ensure scalable support for a growing portfolio
  • Recruit, develop, and mentor a fit-for-purpose internal team, while effectively managing partnerships with CROs and statistical consultants
  • Lead interactions with global regulatory authorities from a statistical perspective, including preparing for and participating in agency meetings (eg, FDA, EMA, PDMA)
  • Anticipate and respond to statistical challenges in BD evaluations, portfolio expansion, and evolving regulatory guidance
  • Represent Biostatistics in governance forums, development leadership meetings and cross-functional initiatives

 

Qualifications:

 

  • Ph.D. required. Biostatistics, Statistics discipline preferred
  • Minimum 15 years of experience in clinical biostatistics within biotech or pharma, including significant leadership in submissions, pivotal trials, and global regulatory interactions required
  • Demonstrated experience providing statistical leadership at the portfolio level across multiple therapeutic areas, preferably including gastroenterology, immunology, dermatology, or neuroscience
  • Strong record of contributions to global regulatory submissions (eg, INDs, NDAs, BLAs), including responsibility for briefing books, response documents, and participation in meetings with health authorities (eg, FDA, EMA)
  • Highly proficient in modern statistical methodologies and tools; hands-on ability when needed in a lean environment
  • Proven success in building and scaling statistical capabilities within high-growth or resource-constrained settings
  • Exceptional communication and collaboration skills, capable of influencing senior stakeholders, leading matrixed teams, and navigating ambiguity
  • Experience in business development assessments and integration of statistical thinking into asset evaluations is a plus
  • Deep understanding of the role of biostatistics in shaping global clinical and regulatory strategy, not just execution
  • Thrive in a matrix and lean organization and comfort working across multiple stakeholders and geographies

 

The range of starting base pay for this role is 271K – 374K.  Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan.

 

 

Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, , Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts.

 

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We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.