Global Clinical Trial Coordinator
1 day ago
Job Requirements: Experienced Clinical Trials Professional
Estimated Salary: $140,000 per annum
The Senior Clinical Trial Manager is an experienced professional with a strong background in clinical trials operations. This individual will oversee clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements.
This role requires strong communication skills for coordinating activities with internal teams, sites, and vendors. The ideal candidate will have a proven ability to build and maintain relationships with clinical trial sites and Principal Investigators.
- Key Responsibilities:
- Planning, implementing, and managing of clinical trials in compliance with industry regulations and ICH-GCP.
- Oversight of CROs and clinical trial sites, ensuring timely delivery, meeting recruitment targets, and producing high-quality data.
- Collaboration with teams for efficient study start-up, identifying risks and ensuring timelines are met.
- Subject matter expert on assigned protocols and management of CRO/site during start-up activities, including contract negotiations and document collection.
- Consistency in Clinical Operations processes across trials and regions.
- Work cross-functionally with departments to meet study requirements and timelines.
- Contribution to developing and reviewing study-related documents and deliver trial-specific training.
- Monitoring open action items and data trends, addressing issues with CROs to enhance study execution and efficiency.
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