Clinical Research Administrator

Há 3 dias


Lisboa, Lisboa, Portugal Iqvia Argentina Tempo inteiro

**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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