Review key study documents produced by other functions (protocols, statistical analysis plans [SAPs], TFL shells, case report forms) and interact with Statisticians and other clinical team members to ensure programming requirements are understood. Follow SAPs, develop specifications and execute derivation algorithms for analysis dataset production. Follow the SDTM and ADa

The individual in this position will perform a variety of manufacturing technician and low level engineering design activities in support of Glaukos' ocular related products manufacturing activities. Responsibilities include building subassembly and top level assemblies for Glaukos stent systems, developing creative solutions to manufacturing problems, ensuring the proper

Quality System Interfacing with all departments to ensure the quality system is implemented and effective. Lead groups in improvement projects to ensure continued compliance of the quality system. Creating reports in Oracle Cloud and CATSWeb systems for CAPA Review Board, Management Review, CAPAs, and other trending requests. Maintaining existing modules within the Oracle

How will you make an impact? The Receptionist is the first impression of the Glaukos corporate campus. They are the host to our guests, clients, and board members. The Receptionist will act as a brand ambassador whose primary focus is to welcome and direct our guests at the front desk. This position must be able to juggle a high frequency of incoming phone calls and trans

How will you make an impact? Glaukos is a medical technology and pharmaceutical company that's advancing the treatment of ophthalmic diseases. At Glaukos, we are pioneering new treatments for chronic eye diseases and are focused on novel therapies for the treatment of glaucoma (market leader iStent inject W), corneal disorders and retinal diseases. Glaukos is looking for

How will you make an impact? The Statistical Programmer II generates datasets, tables, listings and graphs to support statistical analyses of data for clinical studies, regulatory submissions and publications. This position requires a basic understanding and ability to provide datasets using current industry standards including Clinical Data Interchange Standards Consorti

Manage and coordinate manufacturing and supply chain activities in support of development, clinical and marketed products. Provide expertise in support of internal qualifications and process validations. Provide expertise in support of qualifications of CRO's, CMO's, CPO's, 3PL's and related vendors in support of product manufacturing and supply chain. Key contributor on

& Work Experience Design Control Working with development teams to assure Clear and concise user requirements, product specifications, plans, verification and validation studies, risk management strategies and other relevant design control deliverables, Test protocols that include qualified and repeatable test methods, appropriate risk based sample sizes and clear test ins

How will you make an impact? The Clinical Data Manager I will, at the direction of the Lead Clinical Data Managers, review data for multiple studies and perform User Acceptance Testing (UAT). Clinical Data Manager I will r ecommend process improvements related to their job responsibilities that can be used or developed to increase efficiency. What will you do? Data Review

Glaukos Area Director Corneal Health (Central) Base $160 185k; Total Targeted Comp $270 300k+ The Cornea Area Director position will cover these states in the Central United States Texas, Wisconsin, Illinois, Indiana, Missouri, Iowa, Nebraska, Colorado, Kansas, and Oklahoma. How will you make an impact? The Area Director Corneal Health Central will be responsible for lead

Glaukos Practice Integration Liaison (Central) Total Targeted Compensation up to $250k How will you make an impact? The Practice Integration Liaison's objective is to improve patient access and experience with the Glaukos family of products by assisting ophthalmology groups remove operational and organization barriers. The Practice Liaison is responsible for the coordinat

Glaukos Practice Integration Liaison (West) Total Targeted Compensation up to $250k How will you make an impact? The Practice Integration Liaison's objective is to improve patient access and experience with the Glaukos family of products by assisting ophthalmology groups remove operational and organization barriers. The Practice Liaison is responsible for the coordination

How will you make an impact? What will you do? The Clinical Research Associate (CRA) is responsible for establishing and maintaining the Study Master File, tracks critical trial information, and supports Regional Clinical Research Associates under the guidance of a Clinical Manager or Clinical Director. Study Master File Maintenance Sets up Study Master File and Study Mas

GLAUKOS SR. MEDICAL SCIENCE LIAISON (North/Midwest) We are a medical technology and pharmaceutical company that's advancing the treatment of ophthalmic diseases. At Glaukos, we are pioneering new treatments for chronic eye diseases and are focused on novel therapies for the treatment of glaucoma (market leader iStent inject W), corneal disorders and retinal diseases. We h

How will you make an impact? The Clinical Programmer II will, at the direction of the Lead Clinical Programmers, design clinical study databases, program edit checks, integrate external data sources, and model and deliver data reports, dashboards and datasets. The Clinical Programmer II works in coordination with the Lead Clinical Programmer, Data Management, Biostatistic