Associate II, TMF Operations (LATAM)

Worldwide Clinical Trials; Argentina; Remote; ARS 30,318,000 - 60,635,000; Full time

Job summary

Worldwide Clinical Trials seeks an Associate II in TMF Operations to maintain trial master file documents, ensuring accuracy and inspection readiness across complex studies. You will take ownership of document processing, review, and quality control activities across sponsor portfolios.

As part of a globally focused team, you will collaborate with Worldwide project teams and work with electronic document management and eTMF systems to support compliant, high-quality trial records that impact

Qualifications

• University degree in life sciences preferred.
• Up to two years of TMF experience in CRO/pharma.
• Proficiency in English with strong written and verbal communication.
• Experience with data collection, indexing, and standardized document naming.

Responsibilities

• Perform TMF Approver and TMF Quality Control Reviewer activities.
• Process, review, and resolve rejected TMF documents for complex studies.
• Manage essential documents in electronic and hard-copy formats.
• Prepare periodic TMF Quality Control checklists for project review.
• Conduct regular quality checks to support regulatory compliance and industry standards.
• Review, classify, index, and process essential documents using electronic systems.
• Apply consistent document naming and filing standards for accurate records.
• Collaborate with global project teams to address documentation issues and support TMF quality.

Skills

Detail oriented

English proficiency

Documentation

Electronic records management

Education

Life science degree

Tools

eTMF systems

MS Word

MS Excel

Document management systems

Job description

Who We Are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

Make an Impact as an Associate II, TMF Operations at Worldwide

Help maintain the quality and integrity of clinical research by ensuring essential Trial Master File documents are accurate, complete, and managed in line with regulatory and industry standards.

You will take ownership of document processing, review, and quality control activities across complex studies or sponsor portfolios. Your attention to detail will support inspection‑ready TMFs and help project teams deliver research that makes a meaningful impact on patients’ lives.

As part of a globally focused team, you will collaborate with Worldwide project teams and work with a range of electronic document management and eTMF systems.

Where You'll Work

This is a remote role open to candidates based in Latin America. You will collaborate with global teams across multiple time zones.

What You'll Do

• Perform TMF Approver and TMF Quality Control Reviewer activities in accordance with relevant procedures and working practices.
• Process, review, and resolve rejected TMF documents for complex studies or sponsor portfolios.
• Manage essential documents in electronic and hard-copy formats.
• Prepare periodic TMF Quality Control checklists for project team review.
• Conduct regular quality checks to support compliance with regulatory requirements, ICH GCP, sponsor expectations, and industry best practices.
• Review, classify, index, and process essential documents using electronic document management and eTMF systems.
• Apply consistent document naming and filing standards to maintain accurate, high-quality trial records.
• Collaborate with global project teams to address documentation issues and support TMF quality.

What You'll Bring

• A university degree is preferred, ideally in a life science discipline.
• Up to one to two years of relevant TMF experience within the CRO or pharmaceutical industry.
• Proficiency in English, with excellent written and verbal communication skills.
• Experience in data collection, document indexing, editing, and standardized document naming.
• Strong attention to detail, with the ability to manage multiple tasks accurately and meet deadlines.
• Effective planning, organizational, and interpersonal skills in a fast‑paced, changing environment.
• Proficiency in Microsoft Word and Excel.
• Familiarity with electronic document repositories or eTMF systems, together with a general understanding of clinical research principles and processes.

We love knowing that someone is going to have a better life because of the work we do.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.