* Lead and oversee global clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements.
* Serve as the primary point of contact for internal and external stakeholders, supporting site initiation, monitoring, and close-out activities.
* Ensure timely and accurate documentation, data collection, and reporting in line with project timelines.
* Collaborate with cross-functional teams including CRAs, Medical Monitors, Regulatory Affairs, and Data Management.
* Contribute to risk-based monitoring strategies and support audit readiness.
* 5 years+ experience in clinical project management, preferably in Oncology.
* Strong knowledge of ICH-GCP and EMA & FDA regulatory environment.
* Proven ability to work independently and manage global clinical operations.
* Excellent communication and organizational skills.
* Eligibility to work as a Freelancer in your country of residence.
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