Senior Principal Biostatistician

Biogen, Inc.; Cambridge (MA); On-site; USD 138,000 - 185,000; Full time

Job summary

An established industry player is seeking a Senior Principal Biostatistician to lead study design and data analysis in clinical development. This critical role involves providing statistical expertise, mentoring junior staff, and contributing to process improvements. You will represent Biostatistics on project teams, define methodologies, and ensure the quality of statistical deliverables. Join a dynamic team dedicated to delivering life-changing medicines while enjoying a competitive salary and comprehensive benefits. If you are passionate about making an impact in the biotech field, this opportunity is for you.

Benefits

Fitness & Wellness Programs

Short- and Long-Term Disability Insurance

Paid Vacation Days

Paid Holidays

Sick Leave

Paid Maternity and Parental Leave

401(k) with Company Match

Employee Stock Purchase Plan

Tuition Reimbursement

Qualifications

• PhD in Biostatistics or Statistics with 3+ years of experience.
• Thorough understanding of statistical principles and clinical trials.

Responsibilities

• Lead study design and data analysis for clinical development.
• Provide statistical expertise and mentorship to junior biostatisticians.

Skills

Statistical Analysis

Clinical Trial Methodology

SAS Programming

Technical Problem Solving

Communication Skills

Project Management

Education

PhD in Biostatistics/Statistics

Tools

SAS

Statistical Computing Tools

Job description

The Senior Principal Biostatistician is responsible for leading study design and data analysis and providing statistical expertise for company products within one or more therapeutic areas in clinical development. They act as an independent SMT or RDPT Biostatistician, provides statistical input in the scientific discussion, participates in protocol development, analysis plans and file/report specifications, and reviews study setup activities including but not limited to randomization, CRFs and serves as lead biostatistician to assigned project(s). This person performs statistical analyses, interprets statistical results, and prepares clinical study reports including integrated summaries for submissions as appropriate. They also assist in the preparation of responses to statistical issues arising in regulatory or other legal settings, or from external development partners. They maintain liaison with clinical research personnel in order to identify and meet the statistical support required by the development strategy under the supervision of the Associate Director or Director. They also contributes to the long-term growth strategy of the department by participating in process improvement initiatives, keeping abreast of the current statistical methodology development, and providing mentorship to new/junior biostatisticians.

What You’ll Do

• Represent Biostatistics on Project or Study Teams; provides statistical expertise to support clinical development, objectives and strategy
• Defines statistical methodology, analyzes data and reports results and contributes to the strategic planning and execution of the clinical development plan for the assigned project; trains and supervises contract statisticians and ensures the quality of their deliverables.
• Assists responses to addressing statistical issues are part of regulatory, legal or other challenges to the company’s products or processes; may represent Biostatistics in key meetings as assigned
• Serves as peer reviewer for material authored or coauthored by other statisticians and other clinical research personnel, and acts as an internal consultant, as assigned, on broad statistical issues that impact on the pharmaceutical/Biotechnology industry
• Participates in approved process improvement initiatives; mentors new/junior biostatisticians; keeps up to date current on statistical methodology and computing development. Conducts modelling and simulations as needed.

Qualifications

Required Skills

• PhD in Biostatistics/Statistics or equivalent with a preferred 3+ years relevant work experience as Biostatistician in clinical trials
• Thorough understanding of statistical principles and clinical trial methodology with the ability to practice and implement them.
• Ability to provide technical solutions to a wide range of difficult problems. Solutions are innovative, thorough and practicable, and consistent with objectives.
• Working knowledge of medical/biological terminology and clinical trial designs and competitive landscape in relevant therapeutic areas.
• Conversant with SAS or other software programming, and detailed knowledge of SAS procedures as well as computing tools for modelling and simulations.
• Working knowledge of regulatory guidelines and Commercial needs relating to statistical analysis, study reports and statistical components of regulatory submissions for clinical trials.
• Able to manage multiple projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change.
• Able to write and present information effectively. Demonstrates leadership skills with effective communication including being able to explain methodology and consequences of decisions in lay terms; able to translate requests to meaningful and relevant hypotheses/statistical questions.

Additional Information

The base salary range for this position is $138,000 - $185,000.Base salary offered isdetermined though an analytical approach utilizing a combination of factorsincluding, but not limited to, relevant skills & experience, job location, and internal equity.Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees and theirfamilies'physical, financial, emotional,andsocial well-being;including, but not limited to:

• 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 days off for Personal Significance
• 80 hours of sick timeper 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

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.