Data Manager for Clinical Trials
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About the role
Hybrid clinical data management role in Buenos Aires supporting clinical research projects. Responsibilities include database setup and testing, eCRF and data management plan development, data validation, medical coding, SAE reconciliation, database lock metrics, audits, and training. Requires a college or university degree, demonstrated clinical or medical data management experience, English proficiency, clinical data management systems experience, and MS Office proficiency.
Key requirements
- • College/University degree (Life Science, Pharmacy degree is a plus)
- • Required skills: Demonstrated experience managing clinical or medical data, Clinical Data Management systems, such as Medidata Rave or Oracle InForm, Microsoft Office applications, Organisational and time management, Ability to work independently and multitask, English proficiency
- • Required language: English
Opportunity details
- • Workplace: Hybrid
- • Posted: Jun 10, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Data Manager for Clinical Trials
Location: Buenos Aires, Buenos Aires, Argentina
Employment type: Full-time
Workplace type: Hybrid
Company Description
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.