Worldwide Clinical TrialsArgentina, Santiago del Estero, Argentina · Remote Solely
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 ta…
Skills: TMF Operations, Clinical Research, Document Management, Quality Control, Regulatory Compliance
Argentina, Santiago del Estero, Argentina · Remote OK
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical de…
Skills: Clinical trial payments, Budget administration, Clinical operations, Project management, Vendor oversight
Argentina, Santiago del Estero, Argentina · Remote OK
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical de…
Skills: Clinical trial knowledge, Budget configuration, Payment systems, Excel, Project management
Argentina, Santiago del Estero, Argentina · Remote OK
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical de…
Skills: Clinical trial payments, Project management, Budget administration, EDC systems, Vendor oversight
Argentina, Santiago del Estero, Argentina · Remote OK
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical de…
Skills: Clinical trial knowledge, Excel, Project management, Communication skills, Attention to detail
Argentina, Santiago del Estero, Argentina · Remote Solely
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description To be completed by HR/TA.
Skills: Clinical Trial Coordination, Clinical Research, Project Management, Regulatory Compliance, Data Management
Argentina, Santiago del Estero, Argentina · Remote Solely
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Latam Spanish Language Specialist Thermo Fisher Scientific Language Services is looking for a Latam Spanish Language Specialist with exper…
Skills: Clinical translation, Quality assurance, Terminology management, Style guide development, CAT tools
Worldwide Clinical TrialsArgentina, Santiago del Estero, Argentina · Remote Solely
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 ta…
Skills: Trial Master File, TMF Operations, Document Management, Clinical Research, Data Collection
Argentina, Santiago del Estero, Argentina · Remote Solely
If you have a Candidate Login already, but have forgotten your password please use the steps to reset your password. If you have forgotten your email login, please contact [email protected] subject Workday Candi…
Skills: Translation, Copy-editing, Localization, Spanish Latam Fluency, English Fluency
Argentina, Santiago del Estero, Argentina · Remote Solely
Company Description Vialto is a market leader in Global Mobility Services. Our purpose is to “Connect the World.” We are unique and the only stand-alone global mobility business. This presents a rare opportunity for our …
Skills: HR Operations, Workday, Employee Lifecycle Management, Payroll Coordination, HR Policy Guidance
Worldwide Clinical Trials
Argentina, Santiago del Estero, Argentina • Remote Solely
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The role involves processing, reviewing, and maintaining Trial Master File (TMF) documents in accordance with SOPs and regulatory standards. You will perform quality control reviews and collaborate with project teams to ensure document accuracy and compliance.
Candidates should have 1-2 years of relevant TMF experience within the CRO or pharmaceutical industry. A university degree, preferably in Life Sciences, is desired along with proficiency in Microsoft Office and document management systems.
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.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
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!
TMF Operations handles the processing, maintenance and archiving of all essential documents in strict accordance with pertinent Standard Operating Procedures, country-specific regulations, and industry best practices. Throughout Worldwide Clinical Trials, our culture of collaboration and innovation is what propels us in our pursuit of excellence in clinical research and making a meaningful impact on every patient's life. Roles within our TMF Operations department have a global scope, with the opportunity to regularly collaborate with members of the Worldwide Project Team.
Fulfil the "TMF Approver" and/or "TMF QC Reviewer" roles as defined by the relevant Standard Operation Procedure(s) (SOP) and working practices.
Process, review, and resolve rejected Trial Master File (TMF) documents, for complex studies or Sponsor portfolio of studies both in an electronic and hard copy format.
Prepare periodic TMF Quality Control checklists for review by Project Team review.
Perform periodic TMF Quality Control to ensure adherence to regulatory, ICH GCP, Sponsor, and industry best practices.
Work with a variety of Electronic Document Management and electronic TMF Systems to review, classify and process Essential Documents
Possess data collection, indexing and editing skills, including ability to adhere to standardized document naming conventions
Possess excellent written and verbal communication skills to clearly and concisely present information
Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment
Handle multiple, highly detailed tasks with exceptional accuracy. Demonstrate strong planning and organizational skills
Demonstrate proficiency in Microsoft Word and Excel
Develop proficiency in use of an electronic document repository or eTMF. General understanding of clinical research principles and processes
University Degree preferred (Life Science desirable)
Up to 1-2 years of relevant TMF experience within the CRO/Pharma industry
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
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.
Worldwide Clinical Trials (Worldwide) is a global CRO serving development-driven biopharmaceutical companies, with more than 4,400 professionals operating across more than 70 countries. The company delivers therapeutically dedicated expertise in neuroscience, oncology, rare disease, and internal medicine, with comprehensive support across every development phase – from early-stage and first-in-human studies through Phase III registration trials. The company's flexible service model – spanning full-service trial management to functional service partnerships through Worldwide Flex – is powered by a people first, partnership driven outsourcing approach that strengthens collaboration, enhances data transparency, and supports more informed decision making. This provides sponsors with tailored, adaptable solutions that keep pace with the evolving demands of clinical research. Learn more at www.worldwide.com
Offices: 600 Park Offices Drive, Suite 200, Research Triangle Park, NC 27709, US · 2455 Northeast Loop 410, Suite 150, San Antonio, TX 78217, US · 4509 Freidrich Lane, Building 2, Suite 200, Southpark Commerce Center Two, Austin, TX 78754, US · 245 First Street Riverview II, Suite 1847, Cambridge, MA 02142, US · 4.1 Manuel Ugarte 2110, CABA, Buenos Aires, 1428, AR
There are currently 10 open administrative positions in Argentina, Argentina listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Parexel, Thermo Fisher Scientific, Worldwide Clinical Trials, Vialto, Welocalize, among others. Browse the listings above to see every active employer.
Yes — 10 of the 10 open administrative positions offer remote or hybrid work (10 remote, 0 hybrid).
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