Data Manager for Clinical Trials

PSI CRO·Riga, Latvia

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About the role

PSI seeks a Data Manager for Clinical Trials in Riga to manage clinical or medical data across database setup, eCRF and plan development, validation, coding, SAE reconciliation, quality checks, audits and database lock activities. The role involves communication with clients, project teams and vendors, staff training, and requires a college or university degree, 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: Clinical or medical data management, Clinical Data Management systems, such as Medidata Rave or Oracle InForm, Microsoft Office applications, Database setup, testing, maintenance and data entry, Electronic case report form (eCRF) design, Data Management and Data Validation Plan development, Data validation and manual CRF review, Serious adverse event (SAE) reconciliation, Medical data coding, Database quality control checks, Clinical data management working files, Audit preparation and participation, Clinical trial data management training, English
• Required language: English

Opportunity details

• Workplace: Hybrid
• Posted: Jul 10, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Data Manager for Clinical Trials

Location: Riga, Latvia

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.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

Job Description

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.

Please submit your CV in English

Responsibilities will include:

Track database set-up, testing, maintenance and data entry
Communicate with clients, project teams and vendors on data management matters
Review study documents, design and develop project specific guidelines and instructions
Design eCRF, Data Management and Data Validation Plans and test EDC databases
Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation
Code medical data
Track and report metrics leading to database lock
Coordinate the processing, dispatch and archiving of CRFs/queries
Maintain Clinical Data Management working files
Perform database QC checks, prepare and attend audits
Train site staff and project teams on CRF completion and data management topics

Qualifications

College/University degree (Life Science, Pharmacy degree is a plus)
Demonstrated experience of managing clinical or medical data
Full working proficiency in English
Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)
Proficiency in MS Office applications
Organisational and time management skills
Ability to work independently and multi-task

Additional Information

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.