Additional Location(s): US-CA-Valencia; US-CA-Carlsbad; US-CA-Central Coast; US-CA-Central Valley; US-CA-Chico/Eureka; US-CA-Fremont; US-CA-Irvine; US-CA-Laguna Hills; US-CA-Long Beach; US-CA-Los Angeles; US-CA-Los Gatos; US-CA-Menlo Park; US-CA-Modesto; US-CA-Mountain View; US-CA-North Bay; US-CA-Oakland/East Bay; US-CA-Orange County; US-CA-Sacramento; US-CA-San Bernardino/Palm Springs; US-CA-San Bruno; US-CA-San Clemente; US-CA-San Diego; US-CA-San Francisco; US-CA-San Jose; US-CA-Santa Barbara; US-CA-Santa Rosa; US-CA-Silicon Valley; US-CA-Stockton; US-CA-Sunnyvale; US-CA-Turlock; US-CA-Ventura County

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing – whatever your ambitions.

**This role requires hybrid (three times a week) at our Valencia, CA location.**

About this role:

The Senior Biostatistician is responsible for applying statistical and research methodological principles to the design, execution and analysis of clinical studies. Primary emphasis is on supporting clinical studies to assess the safety and efficacy of medical devices manufactured and distributed by BSC Neuromodulation team and analyzing clinical study data. This Senior level position will contribute to process improvement efforts in the statistics department as well as clinical division.

Your responsibilities will include:

⦁ Serves as a key partner and interacts regularly with clinical study teams in clinical trial design, evidence planning, and publications.

⦁ Supports the design of clinical trials, including the recommendation of appropriate research design, sample size considerations, measurements of outcome variables, data collection forms design, expected data analysis/statistical procedures to be used, etc.

⦁ Supports the development and documentation of the study protocol with primary responsibility for study design, which includes the statistical hypotheses, sample size, and analysis plan for meeting the study objectives.

⦁ Supports the writing of statistical analysis plans for clinical trials.

⦁ Assists with the development and review of case report forms to ensure data will be collected efficiently and effectively.

⦁ Conducts statistical analysis and interpretation of clinical trial data and prepares reports to be submitted to the U.S. Food and Drug Administration and other regulatory bodies.

⦁ Assists others in Regulatory and Clinical Affairs with data retrieval that will facilitate the monitoring of clinical trials.

⦁ Participate in the preparation of abstracts, oral and poster presentations, and publications relating to the results of clinical studies. Respond to requests from clinical study investigators for statistical support with study design and data analysis.

⦁ Interact with the clinical study investigators to determine optimal approaches for analyzing and interpreting data for publication and presentation.

⦁ Participate in process improvement efforts to improve the efficiency of study conduct, data management, and data quality processes in clinical studies.

⦁ Remain current on start-of-the-art statistical methods useful in clinical trial design and analysis, mentor junior level biostatisticians.

⦁ Participate in the education of field support staff, clinical study investigators, study coordinators, and in the organization and presentation of materials for investigator site meetings; in addition, to participate in investigator meetings during the course of the study to discuss the clinical status of the study.

⦁ Responsible for practicing Quality System Manual procedures and complying with its requirements, and carrying out responsibilities as outlined in safety, health and environmental policies.

Required qualifications:

⦁ Minimum Master's degree required in Biostatistics or related field

⦁ Minimum 3 years of experience in design and analysis of clinical studies, or minimum 1 year experience with a Ph.D. degree

⦁ Proven, strong applied statistical skills

⦁ Advanced SAS programming skills

Preferred qualifications:

⦁ Proficiency with FDA requirements and procedures for advisory panel meetings and PMA approvals

⦁ Proficiency with PC database and statistical software such as SAS, etc.

⦁ R and/or Python experience is a plus

Requisition ID: 587509

The expected annualized base pay range this full-time position working at this location will be from $91,500 to $173,800 plus annual bonus (subject to plan eligibility and other requirements) and the value of core and optional employee benefits being offered at BSC, which can be reviewed at At BSC, it is not typical for an individual to be hired near the bottom or top of the pay range. Boston Scientific considers various factors in determining actual compensation for this position at the expected location. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs. Actual compensation may be otherwise adjusted if the position is filled outside of the intended geographic location.

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you

At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer.

Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code § , Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination.