TMF Records Associate – RMC Operations (Entry‑Level)

Worldwide Clinical Trials Limited; Argentina; Remote; ARS 420,000 - 640,000; Full time

Job summary

Worldwide Clinical Trials Limited in Argentina seeks a Records Management Compliance professional for the TMF Operations team. You will process, review, and resolve TMF documents, maintain electronic systems, and support the RMC Lead to ensure regulatory compliance across studies.

Excellent written and verbal communication, attention to detail, and familiarity with standard procedures are essential. This role offers an opportunity to advance within a globally respected CRO and contribute to

Qualifications

• University degree preferred.
• Minimum 6 months of TMF experience or similar in regulated environments.
• Knowledge of CRO/Pharma regulatory principles and documentation handling.

Responsibilities

• Fulfil the TMF Approver role as defined by SOPs and working practices.
• Process, review, and resolve rejected TMF documents across studies.
• Work with electronic TMF systems to review, classify and process Essential Documents.
• Communicate trends and issues to the RMC Lead.
• Escalate TMF quality issues to the RMC Lead promptly.
• Provide admin support for the RMC Lead including filing and trackers.

Skills

Data collection

Indexing

Editing

Communication

Attention to detail

Education

University Degree preferred

Tools

eTMF systems

Electronic Document Management Systems

Microsoft Word

Microsoft Excel

Job description

Worldwide Clinical Trials Limited in Argentina seeks a Records Management Compliance professional for the TMF Operations team. You will process, review, and resolve TMF documents, maintain electronic systems, and support the RMC Lead to ensure regulatory compliance across studies.

Excellent written and verbal communication, attention to detail, and familiarity with standard procedures are essential. This role offers an opportunity to advance within a globally respected CRO and contribute to