Clinical Trials Associate - Multiple Levels

The Clinical Trials Associate is responsible for the coordination of clinical research studies in compliance with U.S. and international regulations under the guidance of a Clinical Manager or Clinical Director.Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients. Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra “We’ll Go First,” which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol “GKOS”. Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.How you will make an impact:The Clinical Trials Associate II is responsible for the coordination of clinical research studies in compliance with U.S. and international regulations under the guidance of a Clinical Manager or Clinical Director.What you will you:Clinical Trials CoordinationAssists with the development of clinical trial protocolsReviews clinical study dataAssists with development of case report formsCTA is responsible for effective communication with clinical trial sitesAnalyses of study data with support of more experience CTAs or managerReviews and Monitors Clinical Study DataReviews data as it comes in from sitesDocuments errors and communicates to Manager and Director Clinical OperationsCommunicates with sites to correct errorsAssists Manager with study managementStudy Master File MaintenanceSets up Study Master File and Study Master File Tracker at the beginning of each studyReceives, QC’s, scans and files documents in Study Master FileProvides status of documents to Clinical ManagementCollection of Site Start-Up DocumentsCommunicates directly with site staff to obtain site start-up documentsPrepares Regulatory Binders and provides to sites prior to Site Initiation Visit (SIV)Obtains site documents from Regional Clinical Research Associates during trialReceives, QC’s, scans, and files site documents in Study Master FileProvides status of site documents in Study Master File to Regional Clinical Research Associates prior to Monitoring VisitsEstablishes and Maintains Tracking of Critical Trial InformationTeam and site contact informationSite status informationEnrollment trackersAdverse event trackersSite payment trackers and site payments Team SupportSchedules meetings, set up of AV, teleconference or video conference equipmentPreparation of relevant materialsSupport IP shipment and shipment of other materials to sitesHow You’ll Get There:Bachelor's Degree with background in science, or equivalent work experience preferred2 or more years clinical work experience in the bio- pharmaceutical or device industry, preferably within the ophthalmology field CTA must demonstrate the following: Understanding of required regulatory documents for the study. Effective communication and understanding of the role with sites; with both monitors and CRMs.Study start up/site initiation experience a mustThis role works onsite in Aliso Viejo, CA#GKOSUSFull timePosting Date: 2026-07-27