Senior Clinical Research Associate - Early Development

November 6

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• Senior Clinical Research Associate responsible for conducting monitoring activities for client studies. • Performs monitoring according to GCP, ICH, CFR, and client SOPs. • Performs site management activities and monitoring clinical trial quality. • Conducts site qualification, initiation, interim, and close-out visits. • Ensures sites meet performance expectations related to recruitment, enrollment, and retention. • Maintains ongoing communications with site personnel and assists with problem solving.

Requirements

• Minimum of 5 years relevant industry experience • Analytical problem-solving experience, trouble shooting and resourcefulness • Working knowledge of clinical drug development process • Effective communication, interpersonal skills, and the ability to build relationships • Familiarity with medical and clinical trial terminology • Proficient in written and spoken English required • Proficient in local language, as applicable, preferred • Proficiency in widely used technologies • Ability to learn client applications • Travel to be inclusive of regional, national and international as required