Clinical Trial Assistant - S

Responsibilities

• Familiar with clinical trial and drug development process.
• Ability to work in clinical planning and tracking systems, and to learn new systems readily.
• Strong computer skills (EXCEL, MS Word) required. Knowledge of project reporting tools, preferred.
• Demonstrated proficiency in applying basic principles and procedures for resource management, project planning / tracking, and clinical trial management.
• Strong understanding of interdependencies of various clinical databases and implications on business process when databases are changed.
• Great attention to accuracy and detail. Comfortable with data in table / report format.
• Good communication, organizational, and tracking skills. Customer focused.
• Ability to work with cross-functional teams, meet timelines and work independently.
• Thorough understanding of clinical trial conduct and regulation.

Education

Bachelor degree or equivalent education / degree in life science / healthcare is preferred OR If no degree, 3 years clinical Trials experience required, such as in clinical development, drug development or project management with experiencing work in clinical planning and tracking systems.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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