Clinical research associated Full-time Job

The role: • Independent, proactive work to set up and monitor studies, complete reports and maintain documentation clinical research associate • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions clinical research associate • Balancing sponsor generated queries clinical research associate • Taking responsibility for study cost efficiency clinical research associate • Preparation and review of study documentation and feasibility studies for new proposals clinical research associate   • Potential to assist in training and mentoring fellow CRAs You will need: • 24 months+ of monitoring experience in phase I-III trials as a CRA clinical research associate • College degree in medicine, science, or equivalent clinical research associate • Previous monitoring experience in medium-sized studies, including study start-up and close-out • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data • Excellent written and verbal communication in English and local lan