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AtriCure
Mason, OH; Minnetonka, MN; United States of America
Source: AtriCure careers · View original posting
From AtriCure's posting. “We” and “our” refer to the employer.
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. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.
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.
Reporting to the Vice President, Clinical Affairs and Biometrics, the Senior Principal Statistician is responsible for providing Statistics/Statistical Programming services. The Senior Principal Statistician will work 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.
This individual will be responsible for statistical programming deliverables: SAP, derived datasets, Tables, Figures and Listings.
The Senior Principal Statistician will establish and ensure 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.
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
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. Expertise in medical device product development and experience interacting with regulatory agencies highly desirable
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