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
November 8
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
• Conduct qualification visits, site initiation visits, monitoring visits and termination visits • Oversee integrity of the study and utilize problem-solving skills • Review the performance of the trial at designated sites • Develop patient recruitment strategies • Evaluate the quality and integrity of the reported data • Monitor the completeness and quality of Regulatory Documentation
• Site Management or equivalent experience in clinical research • Understanding of clinical trials methodology and terminology • Experience working in Oncology Trials • Ability to perform all clinical monitoring activities independently • Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline • Strong interpersonal, written, and verbal communication skills • Experience working in a self-driven capacity • Client-focused approach to work • Ability to manage multiple tasks • Honest and ethical work approach
• Bonus incentive program • Opportunity to work within multiple therapeutic areas • Career advancement opportunities
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