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We are working with a fast growing organization who are seeking to bring on experienced Senior Clinical Trial Manager to join their team. The position will provide leadership, mentoring, and technical support to the Clinical Operations team to ensure quality deliverables and achievement of milestones and financial goals.
Responsibilities:
Lead the strategic planning and operational delivery of assigned clinical studies and programs across all phases of study management, ensuring compliance with quality standards, regulations, timelines, and budgets.
Oversee the identification, initiation, and engagement of clinical study sites to support effective patient recruitment and retention.
Ensure timely, high-quality site management and clinical monitoring deliverables for sponsors, sites, and vendors using CTMS, eTMF, and tracking tools.
Provide oversight and quality control for study set-up and ongoing maintenance in CTMS and TMF.
Deliver initial and ongoing project-specific training for study teams, leveraging therapeutic expertise as needed.
Requirements:
Bachelor’s degree or RN in a life science or related field of study.
8 - 10+ years of clinical research trial and/or monitoring experience.
Thorough knowledge of ICH-GCP guidelines and applicable regulations.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Other, and Project Management
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Research Services
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