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Job #03114

About our client Our client is a privately held global CRO serving the pharmaceutical and medical device industry. They have a strong foundation of clinical, process and systems expertise. Position Location Clinical Research Associate Texas 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 9) Manage clinical projects overseas Requirements 1) Bachelor's degree or higher with experience in relevant field 2) Knowledge of GCP and regulatory compliance 3) Effective communication skills for interaction with CROs 4) Ability to work in a team as well as independently 5) Willingness and ability to travel to India