Associate Data Manager (Clinical Data Management)

Location: Budapest, Hungary

Employment: Full time

Company

hirify.global, part of Thermo Fisher Scientific, provides clinical technology and data solutions that help transform clinical trial evidence and accelerate life-changing therapies.

What you will do

• Perform quality control and consistency checks across source data, edit check outputs, and final deliverables.
• Investigate data discrepancies and coordinate resolution with Data Managers, scientific teams, medical staff, project teams, and clients.
• Support the creation, review, and maintenance of Data Management Plans, Data Transfer Specifications, reports, templates, and study records.
• Coordinate edit checks, transfer schedules, reconciliation activities, final data transfer requirements, and study tracking updates.
• Maintain audit-ready documentation and support metrics, CAPA activities, and continuous improvement initiatives.
• Communicate study status and data-related updates to internal teams, project leadership, and clients.

Requirements

• Bachelor’s, Master’s, or PhD in Life Sciences, Healthcare, Pharmaceutical Sciences, Clinical Research, Data Science, or a related field, or equivalent practical experience.
• Foundational understanding of Clinical Data Management and clinical trial protocols, study documentation, and sponsor requirements.
• Strong analytical, organizational, problem-solving, communication, and attention-to-detail skills.
• Ability to manage multiple priorities and deliver high-quality work in a deadline-driven environment.
• Ability to work effectively within cross-functional global teams.
• Knowledge of GCP, FDA, EMA, or other applicable regulatory requirements is preferred.

Nice to have

• Experience in pharmaceutical, biotechnology, healthcare, life sciences, or clinical research environments.
• Exposure to eCOA, ePRO, eConsent, RTSM/IRT, or related eClinical systems.
• Experience with SAS, SQL, or other data analysis and reporting tools.
• Knowledge of CDISC standards, including SDTM.
• Previous experience as a Clinical Research Associate, Study Coordinator, Project Assistant, Project Coordinator, Clinical Trial Assistant, or in a similar role.

Culture & Benefits

• Competitive compensation and incentives.
• Private medical coverage and MetLife protection.
• SZÉP Card and telework reimbursement.
• Flexible time off.
• Employee events and hybrid technology support.