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
Yesterday
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
• The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites. • The CRA works in close collaboration with other CRAs and the Local Study Team to ensure that study commitments are achieved in a timely and efficient manner. • The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct. • The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies. • Ensures compliance with Client Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations. • Ensures the sites deliver according to their respective commitment in the individual studies.
• Excellent attention to detail. • Good written and verbal communication skills. • Good collaboration and interpersonal skills. • Good negotiation skills. • Proficient in written and spoken English language required. • Fluency in local language(s) required. • Ability to work in an environment of remote collaborators. • Manages change with a positive approach for self, team, and the business. • Sees change as an opportunity to improve performance and add value to the business. • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time. • Good analytical and problem-solving skills. • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines. • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment. • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.
Apply NowOctober 2
501 - 1000
Site monitor overseeing clinical studies for BeiGene, an oncology company.