Glaukos Practice Integration Liaison (Southeast) Total Targeted Compensation up to $250k #DaretoDream #DaretoLead #DaretoCare 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 L

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

How will you make an impact? The Sr. Biostatistician will be responsible for leading statistical analysis activities for assigned clinical studies. These activities include creating, reviewing, and maintaining statistical sections of the protocol as well as statistical analysis plans, overseeing the performance statistical analyses, providing data interpretation, and part

GLAUKOS SR. MEDICAL SCIENCE LIAISON (Ohio Valley) #We'llGoFirst 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 di

Join Our Growing GPS Glaukos Patient Services Team! #DareToDoMore Reimbursement Liaison Glaucoma (Texas) How will you make an impact? The Patient Reimbursement Liaison team is part of Glaukos Patient Services (GPS), and will serve as experts in payer policies, patient, and provider support to facilitate appropriate patient access services to ensure patients have access to

What will you do? PROVIDE STRATEGIC REGULATORY GUIDANCE TO MANAGEMENT AND INTER DISCIPLINARY PROJECT TEAMS Provide guidance to inter disciplinary project teams on regulatory requirements on projects at Phase 1 to 4 of drug development/life cycle. Represent independently and proactively regulatory requirements and RA departmental positions to core/projects teams. Generate

Glaukos is Growing! Join Our New GPS Glaukos Patient Services Team Founded in 1998, Glaukos is publicly traded ophthalmic medical technology and pharmaceutical company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders and retinal diseases. Our global headquarters is in Aliso Viejo, California, and we have additional

How will you make an impact? Perform a variety of mechanical engineering activities on the ocular related products including product design, concept prototyping, concept testing, early development, clinical builds, manufacturing scale up development and sustaining activities. Responsibilities include developing creative solutions to design and manufacturing problems, ensu

The Principal Quality Engineer , Medical Device position will be based in San Clemente, CA and will directly support the manufacture of innovative ocular medical devices. This role includes verifying successful transfer of products into manufacturing, the review and/or execution of validations (IQ/OQ/PQ), risk management activities, environmental monitoring, supporting qu

The position of Manufacturing Engineer is responsible for supporting manufacturing by developing, qualifying, implementing and maintaining manufacturing equipment, processes and procedures.This individual will also develop and lead projects to improve process efficiencies and cost savings. Job Requirements Support existing manufacturing product lines. Lead, coordinate and

CLINICAL DATA REVIEW AND EXECUTION Authoring of clinical data management documents such as data management plan, CRF completion guidelines, data review guidelines Responsible for the development of eCRF design and annotation, database design specifications and data review listings Responsible in the validation activities such as user acceptance testing (UAT) of clinical d

The Sr. Manager, Clinical Compliance , based in San Clemente, CA will be responsible for developing, leading, implementing and conducting strategies and activities to assure Glaukos Clinical Research remains in compliance with applicable regulations and laws maintaining a constant state of audit readiness. Internal clinical audits Develop an internal clinical audit progra