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
October 11
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
• 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.
• 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.
Apply NowSeptember 23
501 - 1000
Lead research projects in a global organization focusing on health outcomes.
September 20
10,000+
Join Thermo Fisher Scientific as a Clinical Research Associate, ensuring trial compliance.