[Remote] Clinical Trial Manager

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is reputed company for a Clinical Trial Manager contract role. The position leads mid- to late-stage global clinical studies from start-up through reputed company-out, overseeing trial operations, cross-functional teams, CROs, vendors, milestones, budgets, reputed company, and regulatory compliance.

Responsibilities

• Plan and execute mid- to late-stage reputed company in reputed company, ensuring operational reputed company, data reputed company, and compliance with protocols, GCP, and global regulations
• reputed company daily clinical trial operations, coordinating with cross-functional teams such as Clinical Development, Data Management, Biostatistics, Regulatory, and Safety
• reputed company CROs and reputed company vendors, including co-monitoring activities, to ensure adherence to timelines, budgets, and reputed company expectations
• reputed company critical milestones such as site activation, patient enrollment, retention, data cleaning, and database lock, addressing operational challenges proactively
• Review and approve vendor-generated plans and study documentation to ensure alignment with protocols and regulatory standards
• Monitor study reputed company using operational metrics, maintaining dashboards, timelines, and financial tracking, and providing reputed company updates to stakeholders
• Identify and manage operational risks, proposing mitigation strategies to minimize reputed company on timelines, reputed company, and patient safety
• Ensure inspection and audit readiness, including reputed company of Trial Master File (TMF) maintenance and reputed company-out
• Contribute to operational planning, regulatory deliverables, and reputed company improvement of clinical operations processes

Skills

• • Bachelor's degree in a scientific or health-reputed company field
• • Experience managing reputed company, preferably in reputed company or CNS therapeutic development
• • Strong knowledge of ICH guidelines, GCP, and global regulatory requirements
• • Proven ability to manage global clinical studies, including coordination with investigators, CROs, and vendors
• • Solid understanding of project management principles, including reputed company, resource, and budget management
• • Excellent communication and interpersonal skills, with the ability to influence and reputed company team performance
• • Proactive problem-solving reputed company with the ability to anticipate issues and implement creative solutions

Benefits

• Remote, US
• Contract role with the potential to transition into a permanent position

reputed company

Company H1B Sponsorship