Clinical Research Administrator
Há 3 dias
**Job Title:** Clinical Trial Assistant/Start-Up
**Job Summary:** We are seeking a highly organized and detail-oriented individual to support our clinical research team in Argentina. The ideal candidate will have experience in clinical research administration and possess excellent communication skills.
**Responsibilities:**
• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems like Trial Master File.
• 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.
• Coordinate 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.
**Requirements:**
• High School or University Diploma
• Clinical research administrative support experience preferred
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
• Written and verbal communication skills including good command of Portuguese and English language
• Effective time management and organizational skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Basic knowledge of applicable clinical research regulatory requirement, i.E., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training
• Knowledge of applicable protocol requirements as provided in company training
Company: Iqvia Argentina
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