Detail oriented Research Associate II, offering 5 years of exceptional Clinical Research experience managing multiple projects and to effectively meet business requirements. Currently responsible for coordinating and ensuring the integrity of all activities associated with conducting clinical trials that involve multiple sites are in compliance with all local state federal, and international regulatory requirements. Highly-motivated employee with desire to take on new challenges. Strong worth ethic, adaptability and exceptional interpersonal skills. Adept at working effectively unsupervised and quickly mastering new skills.
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