Senior Clinical Research Associate

October 11

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Parexel

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

• Dedicated to one client. • Responsible for all site management and monitoring activities across assigned oncology studies. • Work with industry leaders and subject matter experts. • Opportunity to mentor junior CRAs. • Work with world-class technology. • A pivotal role in the drug development process.

Requirements

• Substantial Site Management experience, with an understanding of the clinical trial methodology and terminology. • Experience in, or willingness to monitor oncology clinical trials. • Experience in independent monitoring, all types of visits. • Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize. • Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

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