Data Manager for Clinical Trials
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About the role
PSI seeks a Data Manager for Clinical Trials in Tallinn to manage clinical and medical data, including database setup, eCRF and data management plan development, validation, coding, reconciliation, quality checks, audits, metrics, and training. Applicants should have a college/university degree, 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, Full working proficiency in English, Experience with clinical data management systems, such as Medidata Rave or Oracle InForm, Proficiency in MS Office applications, Organisational and time management skills, Ability to work independently and multitask
- • Required language: English
Opportunity details
- • Workplace: Hybrid
- • Posted: Jun 30, 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: Tallinn, Harju County, Estonia
Employment type: Full-time
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.