Associate Data Manager
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 18h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 48d ago
The date the source published, not the day we noticed it (2026-08-14). Last seen at its source just now.
We have tracked this listing since 22 Sep 2026 (8 days). The employer's own board has carried it every time we have read it, most recently just now.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
Hungary
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $99.2k–195k/yr
Middle 50% of 34 listings that do state pay — Operations · all levels · Eastern Europe · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
workday employer's own board first seen 8d ago · last seen just now
- location not stated
The listing
Join Clario, a part of Thermo Fisher Scientific and help transform clinical trial data into meaningful insights that accelerate the development of life-changing therapies. As an Associate Data Manager within our eCOA Data Management team in Budapest, you will play a vital role in ensuring the quality, accuracy, and integrity of clinical trial data throughout the study lifecycle. Working alongside experienced Data Managers, Project Teams, and Sponsor stakeholders, you will support data review, reconciliation, documentation, and process improvement activities while gaining valuable experience in clinical data management and eClinical technologies.
What We Offer
Competitive compensation and incentives
Private medical coverage and MetLife protection
SZÉP Card and telework reimbursement
Flexible time off
Engaging employee events and hybrid technology support
What You'll Be Doing
Perform quality control and consistency checks on study data outputs, ensuring accuracy between source data, edit check outputs, and final deliverables.
Investigate data discrepancies and collaborate with Data Managers, scientific teams, and medical staff to facilitate issue resolution and documentation.
Support the creation, maintenance, and review of study documentation, including Data Management Plans (DMPs), Data Transfer Specifications (DTS), and related deliverables.
Coordinate updates to Clinical Data Management task schedules, including edit checks, transfer schedules, reconciliation activities, and final data transfer requirements.
Assist with data management metrics, study tracking activities, and maintenance of accurate study assignment information within applicable systems.
Support the preparation, formatting, and maintenance of data management documents, templates, reports, and presentations.
Serve as a primary point of contact for client reconciliation feedback, ensuring timely investigation, follow-up, and resolution of data-related requests.
Maintain high-quality documentation and audit-ready records relating to reconciliation activities and study data management processes.
Communicate project status updates effectively to internal teams, project leadership, and clients.
Assist in the maintenance, storage, and organization of study documentation throughout the project lifecycle.
Contribute to continuous improvement initiatives focused on workflow optimization, quality enhancement, and process efficiency.
Support Corrective and Preventive Action (CAPA) activities related to study-specific data management processes.
What We Look For
Bachelor’s, Master’s, or PhD degree in Life Sciences, Healthcare, Pharmaceutical Sciences, Clinical Research, Data Science, or a related field, or equivalent practical experience.
Experience within the pharmaceutical, biotechnology, healthcare, life sciences, or clinical research industry preferred.
Foundational understanding of Clinical Data Management principles and the role of data management within clinical trials.
Ability to review, interpret, and understand clinical trial protocols, study documentation, and sponsor requirements.
Knowledge of Good Clinical Practice (GCP), FDA, EMA, and other applicable regulatory requirements preferred.
Exposure to eClinical technologies such as eCOA, ePRO, eConsent, RTSM/IRT, or related clinical systems is highly desirable.
Previous experience in clinical research roles such as Clinical Research Associate (CRA), Study Coordinator, Project Assistant, Project Coordinator, Clinical Trial Assistant, or similar positions is preferred.
Familiarity with SAS, SQL, or other data analysis and reporting tools is highly desirable.
Knowledge of CDISC standards, including SDTM, is considered an advantage.
Strong analytical, organizational, and problem-solving skills with exceptional attention to detail.
Excellent written and verbal communication skills and the ability to work effectively within cross-functional global teams.
Ability to manage multiple priorities and deliver high-quality work in a deadline-driven environment.
At Clario, a part of Thermo Fisher Scientific, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.