Senior Principal Statistician

AtriCure

5d • Onsite

About The Position

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. We foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.

Requirements

• MS/PhD in Statistics, Biostatistics or a related field.
• At least 3-5 years (PhD) or 6-10 years (MS) experience in medical device, biotech or pharmaceutical development.
• Minimum of 2 years of management experience.
• Knowledge of statistical methodology.
• Good communication skills, both oral and written.
• Knowledge of design, data analysis methodology, SAS programming to meet FDA and ICH guidelines.
• Knowledge of programming Tables, Listings and Figures in SAS for FDA submission.
• Good know of SAS, R and Sample size calculations software.
• Ability to work independently.
• Ability to regularly walk, sit, or stand as needed.
• Ability to occasionally bend and push/pull as needed.
• Ability to pass pre-employment drug screen and background check.

Nice To Haves

• Expertise in medical device product development and experience interacting with regulatory agencies highly desirable.
• PhD in Statistics, Biostatistics or a related field with at least of 4 years of experience in medical device, biotech or pharmaceutical development.
• Statistician with comprehensive experience in programming TLFs for regulatory submissions.
• Experience in supporting 510K, IDE, PMA, NDA, BLA, and or CTD submission.

Responsibilities

• Provides Statistics/Statistical Programming services.
• Works closely with regulatory, scientific affairs, health economics, medical affairs and other departments to ensure optimal study designs, data collection and analysis for regulatory agencies and other stakeholders.
• Responsible for statistical programming deliverables: SAP, derived datasets, Tables, Figures and Listings.
• Establishes and ensures compliance with standard processes and industry best practices.
• Supports the design, analysis, and reporting of trial results.
• Develops statistical methodology for studies, including power analysis, randomization schemes, and statistical analysis plan, subgroup analysis, interim analysis, etc.
• Ensures data collection instruments are designed to capture protocol-specified scientific information and study databases.
• Effectively presents statistical concepts, evidence, interpretations, and logical arguments to the project team, management, and regulatory agencies.
• Develops program verification procedures and plans to provide thorough and detailed reviews of documentation and analysis output.
• Delivers appropriate, accurate and understandable line listings and statistical tables, and preparation and review of statistical sections of study reports and submission reviews.
• Programming and validation of derived datasets Tables, Figures and Listings.
• Oversees work of statistical programmer and CRO/vendor deliverables.
• Manages statistics/statistical programming resources to meet assigned project priorities.
• Contributes to development of timelines and budgets across functional teams to ensure timely submissions aligned with our objectives.
• Works in close collaboration with Data Management and contributes to the development of CRFs. DMP and other DM deliverables.
• Provides statistical input and review for APRs, CSRs, publications to ensure the accuracy of the statistical component of scientific reports with high quality.
• Develops and routinely reviews Statistics/Statistical Programming SOPs to ensure adequate processes are in place to manage quality work in line with regulations.
• Participates in regulatory submission process, including IDEs and 510(k).
• Hires, mentors, manages and evaluates activities of statistics/programming personnel as necessary.
• Manages personnel by appropriately delegating assignments, reviewing activities and defining and ensuring review of deliverables so that projects are completed on time with high quality.
• Regular and predictable work performance.
• Ability to work under fast-paced conditions.
• Ability to make decisions and use good judgment.
• Ability to prioritize various duties and multitask as required.
• Ability to successfully work with others.
• Additional duties as assigned.

Benefits

• Medical & Dental beginning day 1 of employment
• 401K plus match
• 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads
• Volunteer Time off
• Pet Insurance
• Full access to our on-site fitness center and cafeteria (for Corporate-based employees)

What This Job Offers

• Job Type: Full-time
• Career Level: Senior