Senior Clinical Trial Assistant & Team Mentor

IQVIA Inc; Buenos Aires; On-site; ARS 64,975,000 - 83,540,000; Full time

Job summary

IQVIA in Buenos Aires, Argentina, seeks a Full-Time Clinical Trial Assistant to support daily administrative activities alongside CRAs and Regulatory and Start-Up teams. You will help update and maintain the Trial Master File, coordinate documentation, and assist with data flow and study file completeness.

The role includes collaboration with the clinical team on documentation handling and archiving, and mentoring junior CTAs. A Life sciences degree and English proficiency are required.

Qualifications

• Bachelor’s degree in Life sciences or related field.
• 1 year in clinical research experience strongly preferred.
• Advanced level of English.
• Computer skills including proficiency in MS Word, Excel and PowerPoint.
• Effective written and verbal communication skills.
• Effective time management and organizational skills.
• Ability to establish and maintain effective working relationships.
• Knowledge of GCP/ICH guidelines as provided in training.
• Knowledge of protocol requirements as provided in training.

Responsibilities

• Assist CRAs and RSU with updating and maintaining TMF documents and systems.
• Collaborate on preparation, handling, distribution, filing, and archiving of clinical documentation.
• Assist with periodic review of study files and completeness.
• Coordinate tracking and management of CRFs, queries and data flow.
• Serve as central contact for the clinical team for communications and documentation.
• Mentor less experienced CTAs and assist with onboarding.

Skills

English proficiency

MS Word

MS Excel

PowerPoint

Communication

Time management

Teamwork

Regulatory knowledge

Education

Bachelor’s degree in Life sciences

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA in Buenos Aires, Argentina, seeks a Full-Time Clinical Trial Assistant to support daily administrative activities alongside CRAs and Regulatory and Start-Up teams. You will help update and maintain the Trial Master File, coordinate documentation, and assist with data flow and study file completeness.

The role includes collaboration with the clinical team on documentation handling and archiving, and mentoring junior CTAs. A Life sciences degree and English proficiency are required.