Clinical Research Associate
3 weeks ago
Clinical Research Associate Role Overview
ICON Clinical Research is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for identifying, selecting, initiating, and closing out investigational sites for clinical studies in phases II – IV.
Key Responsibilities:
- Independent, proactive work to set up and monitor studies, complete reports, and maintain documentation
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor-generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
Requirements:
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- 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
- Ability to work to tight deadlines
- Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
Benefits of Working at ICON Clinical Research:
- Competitive salary packages
- Annual bonuses reflecting delivery of performance goals
- Range of health-related benefits to employees and their families
- Competitive retirement plans
- Life assurance
- Flexible country-specific optional benefits
At ICON Clinical Research, we value diversity, inclusion, and belonging. We are committed to providing an inclusive and accessible environment for all candidates and employees. If you need a reasonable accommodation for any part of the application process, please let us know.
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