Job Overview
Location
Remote, Argentina; Remote, Brazil; Remote, Chile; Remote, Colombia; Remote, Mexico; Remote, Peru
Job Type
Full-time
Category
Other Engineering
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • The Clinical System Administrator provides essential business administration support for sponsor clinical systems, including eTMF/CTMS, IRT, and EDC platforms such as Veeva Clinical Vault and Medidata CTMS, ensuring timely deliverables and user support across Latin America.
- • Day-to-day responsibilities include managing user access for internal, sponsor, and third-party requests; maintaining the Global Directory of sites and institutions; creating and updating studies, countries, and sites within clinical systems; resolving help desk tickets through troubleshooting and issue identification; performing system modifications like picklist and field requirement updates; reviewing clinical system processes and procedures; supporting integrations between clinical and EDC systems; executing archival steps as requested; and assisting leads or managers with ad-hoc tasks.
- • Precision Medicine Group is expanding its operations across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, building a growing team focused on delivering precision medicine solutions through robust clinical trial support and technology enablement.
- • In this role, the individual will deepen expertise in clinical trial systems, gain hands-on experience with Veeva and Medidata platforms, develop cross-functional collaboration skills with IT and project teams, and advance their ability to manage complex system configurations and integrations in a global healthcare technology environment.
🎯 Requirements
- • Degree or equivalent experience in a business, scientific, or healthcare discipline
- • 2 years of clinical trial experience and 2 years of experience with clinical systems (e.g., CTMS, EDC, eTMF, IRT)
- • Professional working proficiency in English
- • Experience with clinical trial systems including requirements gathering, documentation, configuration, and integrations
- • Ability to resolve issues independently with sound judgment and appropriate escalation
- • Strong interpersonal, verbal, and written communication skills
🏖️ Benefits
- • Fully remote work opportunity across multiple Latin American countries
- • Opportunity to work with leading clinical trial technologies such as Veeva Clinical Vault and Medidata CTMS
- • Exposure to global clinical trial operations across diverse regulatory environments
- • Professional development in system administration, integration support, and clinical process management
- • Inclusive workplace committed to equal opportunity employment regardless of background
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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