Clinical Research Coordinator
hace 18 horas
A Clinical Trial Assistant provides administrative support to the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery. Key responsibilities include:
- Assisting CRAs and RSU team with updating and maintaining clinical documents and systems.
- Preparing, handling, distributing, filing, and archiving clinical documentation and reports according to standard operating procedures.
- Maintaining site compliance and performance within project timelines.
Responsibilities
- Track and manage Case Report Forms (CRFs), queries, and clinical data flow.
- Prepare and handle Clinical Trial Supplies and maintain tracking information.
- Act as a central contact for designated project communications and correspondence.
- May accompany CRAs on site visits to assist with clinical monitoring duties.
Requirements
- Life science degree or equivalent combination of education and experience.
- Clinical research experience is highly valued.
- Excellent computer skills including Microsoft Word, Excel, and PowerPoint.
- Effective time management and organizational skills.
- Awareness of applicable clinical research regulatory requirements.
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