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Job #03040

About our client Our client offers a patient-friendly alternative to safely and non-invasively deliver drugs to the eye. They are currently pursuing partnerships with pharmaceutical and biotechnology companies that are marketing or developing products for serious eye diseases. With $15M secured in funding for this year, this is an exciting opportunity for the right candidate to join a fast-paced environment. Position Location Clinical Research Associate Waltham, Massachusetts Salary Highly competitive package, commensurate with experience Responsibilities 1) Supervise and assist in developing and executing clinical research studies in compliance with applicable regulations 2) Execute activities with direction and assistance (as guided by project priorities, timings and quality specifications) 3) Utilize the services of a CRO 4) Assist with writing protocols, clinical study reports, clinical investigational brochures and clinical sections of government submissions 5) Initiate, monitor and closeout clinical studies 6) Ensure timely collection and maintenance of study documentation files and all assigned duties 7) Design, prepare, plan, implement and review clinical trial while ensuring GCP regulatory and ethical standards 8) Organize workload with project priorities and execution Requirements 1) Bachelor's degree or higher with experience in relevant field 2) Knowledge of GCP and regulatory compliance 3) Excellent communication skills (written and verbal) 4) Effective communication skills for interaction with KOLs and CROs 5) Ability to work in a team as well as independently 6) Willingness and ability to travel