Manage planning, execution, progress and completion of clinical projects.
Coordinate with functional experts to ensure regulatory compliance.
Maintain operational, financial and regulatory integrity and safety.
Develop communications, regulatory submissions, audits, and vendor selection as needed.
Lead cross-functional teams for data, documents, SOPs, and tools.
Prepare investigator updates and lifecycle reports.

🎯 Requirements

Bachelor's degree in Health Sciences or Clinical Research; 1-3 yrs PM
Self-motivated with strong communication; results-driven
Strong attention to detail; builds collaborative relationships
Continuous learning and self-development
Ability to foster teamwork
Fluent in English (reading, writing, speaking)

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