Senior CTA: TMF Master & Study Coordination

IQVIA Inc; Tandil; On-site; ARS 49,505,000 - 80,446,000; Full time

Job summary

IQVIA Inc. is seeking a diligent Clinical Trial Assistant to support the CRA and RSU teams in maintaining the Trial Master File and related documentation.

The role emphasizes accuracy, timely updates, and collaboration across study sites to ensure compliance with GCP/ICH guidelines. The ideal candidate holds a life sciences degree, has English proficiency, and is experienced with MS Word, Excel, and PowerPoint.

Qualifications

• Bachelor’s degree in Life sciences or related field.
• 1 year in clinical research experience strongly preferred.
• Advanced level of English.
• Proficiency in Microsoft Word, Excel and PowerPoint.
• Effective written and verbal communication skills.
• Effective time management and organizational skills.
• Knowledge of applicable clinical research regulatory requirements (GCP/ICH).
• Knowledge of applicable protocol requirements.

Responsibilities

• Assist CRAs and RSU team with updating and maintaining TMF and documents.
• Coordinate handling, filing, and archiving of clinical documentation per SOPs.
• Assist with periodic review of study files for completeness.
• Distribute Clinical Trial Supplies and maintain tracking information.
• Coordinate tracking of CRFs, queries and data flow.
• Act as central contact for project communications and documentation.
• Mentor and onboard new CTAs; assist with training.
• May lead CTA study teams or interview potential new hires.
• May accompany CRAs on site visits for monitoring duties.
• Participate in quality or process-improvement initiatives.

Skills

Advanced English

MS Office

Communication

Time management

Relationship building

GCP/ICH knowledge

Protocol knowledge

Education

Bachelor's degree in Life sciences

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

IQVIA Inc. is seeking a diligent Clinical Trial Assistant to support the CRA and RSU teams in maintaining the Trial Master File and related documentation.

The role emphasizes accuracy, timely updates, and collaboration across study sites to ensure compliance with GCP/ICH guidelines. The ideal candidate holds a life sciences degree, has English proficiency, and is experienced with MS Word, Excel, and PowerPoint.