Job Title:
Global Clinical Study Manager
This role will involve managing the delivery of clinical studies from setup to archival, ensuring timely completion and quality standards.
Key Responsibilities
* Evaluate study conduct and progress to identify potential risks or issues that may impact timelines or budgets.
* Develop study plans for external and internal use, including protocols, informed consent forms, monitoring plans, vendor management plans, risk management plans, communication plans etc.
* Maintain interactions with internal teams such as regulatory affairs LOC Quality assurance monitors meetings CROs third-party vendors
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