Centralized Monitoring Lead

4 - 8 years

0 Lacs

Posted:3 days ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Role Overview: You will provide leadership to the centralized monitoring team, working closely with project and clinical leads and other functional teams. Your main goal will be to ensure the successful delivery of projects to the sponsors" satisfaction, optimizing speed, quality, and cost while adhering to standard operating procedures. Key Responsibilities: - Oversee clinical deliverables throughout all trial phases from start-up to close-out. - Develop and review study management plans, risk assessments, and analytics strategies. - Monitor site performance, key risk indicators, and operational triggers. - Coordinate cross-functional teams to meet project milestones. - Ensure quality assurance through regular audits, documentation, and compliance checks. - Lead data review processes and maintain audit readiness. - Provide expertise support in Centralized monitoring studies from Applications, Analytics, and Therapeutics or Quality perspective. - May involve taking up Clinical lead activities, managing finance-related information, project resources, and conducting periodic reviews of site activities. - Act as a mentor or coach for Technical Solution Specialists and monitor site performance to make timely recommendations for corrective actions. Qualifications Required: - Minimum 4 years of CRA and Clinical trials monitoring experience. - Strong knowledge of clinical trial conduct and application of relevant regulatory requirements. - Good command of English language with strong written and verbal communication skills. - Detail-oriented approach with the ability to work on multiple projects and manage competing priorities. - In-depth therapeutic and protocol knowledge. - Bachelor's Degree in clinical, life sciences, mathematical sciences, or related field, nursing qualification, or allied medical degree. Note: The job requires a minimum of 4 years of relevant experience in CRA and Clinical trials monitoring, expertise in clinical trial conduct, and strong communication skills along with a Bachelor's Degree in a relevant field.,

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