Associate Director, Biostatistics

Biogen•San Francisco, CA

1d•$176,000 - $242,000

About The Position

Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey. About This Role: As Associate Director, Biostatistics, you will be at the forefront of leading study design and data analysis, providing statistical expertise for our products across various therapeutic areas. Your role is crucial in clinical development, biomarker development, research, and beyond. Acting independently, you will provide statistical input in scientific discussions, participate in protocol development, and oversee analysis plans and report specifications. You'll play a key role in reviewing study setup activities, ensuring the integrity of randomization and CRFs, and leading biostatistical efforts for assigned projects. Your work involves performing statistical analyses, interpreting results, and preparing comprehensive clinical study reports. Additionally, you'll assist in preparing responses to statistical issues in regulatory or legal settings and liaise with clinical research personnel to align statistical support with our development strategy. Your contributions to process improvement initiatives and mentorship will aid in the long-term growth of our department. This position will report to the Head of Biostatistics for Biogen's West Coast Hub, contributing to exciting late-stage programs in nephrology or new indications in early development.

Requirements

PhD in Biostatistics or equivalent with a minimum of 6+ years relevant work experience in the pharmaceutical/biotech industry.
Thorough understanding of statistical principles and clinical trial methodology.
Ability to provide technical solutions to a wide range of difficult problems.
Conversant with R, SAS, or other statistical software programming languages.
Working knowledge of regulatory guidelines related to statistical analysis.
Strong ability to manage multiple projects and conflicting priorities.
Excellent written and verbal communication skills.

Nice To Haves

Experience with statistical components of regulatory submissions.
Detailed knowledge of R or SAS procedures and computing tools for modeling and simulations.
Proven experience in mentoring junior staff and contributing to process improvements.

Responsibilities

Lead biostatistics representation on project or study teams and provide statistical expertise.
Define statistical methodologies, analyze data, and report results for clinical development plans.
Train and supervise contract statisticians, ensuring quality deliverables.
Assist in addressing statistical issues in regulatory, legal, or other challenges.
Serve as a peer reviewer and internal consultant on broad statistical issues.
Participate in process improvement initiatives and mentor new/junior biostatisticians.
Conduct modeling and simulations as needed.
Collaborate closely with study or project teams for data interpretation and reporting.
Work with statistical programmers, data management, and vendors to deliver analysis results.
Collaborate with medical writers to complete study reports and manuscripts.
Supervise FSP statisticians in assigned tasks.

Benefits

Medical, Dental, Vision, & Life insurances
Fitness & Wellness programs including a fitness reimbursement
Short- and Long-Term Disability insurance
A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
Up to 12 company paid holidays + 3 paid days off for Personal Significance
80 hours of sick time per calendar year
Paid Maternity and Parental Leave benefit
401(k) program participation with company matched contributions
Employee stock purchase plan
Tuition reimbursement of up to $10,000 per calendar year
Employee Resource Groups participation