Local Clinical Trials Assistant
hace 3 días
**Are you a brave mind?**
It takes insight, curiosity, and intellectual courage to transform healthcare. It takes brave minds. By reimagining a world without the consequences of disease, brave minds bring powerful ideas to reality. Not intimidated by complexity, they see possibilities and explore the improbable.
Join us as a **Clinical Trials Assistant**
**What You´ll Do**
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
**What Will Help You Succeed**
- Graduated or currently pursuing a Bachelor´s Degree
- 1/2 years of administrative support experience or equivalent combination of education, training and experience.
- Basic knowledge of applicable clinical research regulatory requirement and clinical research terminology.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
**Unleash your potential to drive healthcare forward
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