Skilled Clinical Research Associate with an international track record of success in progressively responsible positions in clinical environments. Experienced in monitoring multiple site locations, clinical site evaluation, initiation, maintenance and close/out visits in accordance with GCP and company SOPs, while ensuring integrity and study data including following study timelines. Skilled in applying applicable clinical research regulatory requirements such as GCP and ICH guidelines.
Clear awareness of diverse backgrounds alert to widely varied patient needs and circumstances. Collaborative team player, acting as key resource to colleagues and allied health professionals. Consistently meet/exceed expectations, combining cost consistently with quality improvement and customer service.
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