IQVIA is looking for a Centralized Monitor to manage the execution of assigned clinical studies from initiation through closeout. In this home-based role, you will ensure deliverables are on time and in accordance with SOPs, policies, and regulatory requirements. You’ll provide project support across multiple studies, review structured clinical data, and be a key player in maintaining data integrity and subject safety.

What You'll Do

Manage assigned sites and perform Subject Level Data Review independently.
Perform remote monitoring visits and review data to investigate accuracy of inclusion/exclusion criteria, IP, AEs, labs, endpoints, and SAEs.
Perform study-specific analytics and contribute to developing new analytics proposals.
Manage operational insight of assigned sites/studies and complete study/site metrics trending.
Provide inputs to clinical study teams for process improvements and issue escalation.
Identify value adds from centralized review and remote monitoring.
Support CMS leads in performing oversight on clinical deliverables.
Collaborate with project resources including CRAs, CTAs, and the Centralized Monitoring team.
Ensure complete and accurate documentation of site-specific tools and templates.
Perform centralized monitoring activities to evaluate site quality and integrity.
Ensure accurate completion of internal systems, databases, and tracking tools.
Perform management of triggers and preparation of i-site packs.
Act as a backup for relevant stakeholders within the project team.
Conduct periodic review of site-level KRIs and historic site performance.
Monitor site performance and recommend timely corrective actions.
Review effectiveness of recommended actions.
Work in accordance with the Study Central Monitoring Plan.
Establish and maintain effective project and site-level communications.
Provide mentorship to Associate Central Monitors.
Review reports, identify issues, escalate to Clinical Lead, prepare annotations, and conduct CRA trainings.
Act as a technical solution specialist (TSS) point of contact.
Analyze requirements complexity and provide EAC hours and turnaround time.
Review the Study Central Monitoring Plan.
Attend Kick-Off meetings, weekly team meetings, and client meetings as needed.
Adhere to key activities outlined in the SOW per customer requirements.

What We're Looking For

Bachelor’s degree in clinical, life sciences, mathematical sciences, a related field, or a nursing qualification.
Minimum of 2 years of relevant work experience or an equivalent combination of education, training, and experience.
Freshers with a Medical or Allied medical degree are also encouraged to apply.
Advanced knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements (ICH GCP, local laws, regulations).
Good Clinical system expertise.
Strong written and verbal communication skills including a good command of the English language.
A good command of the Hungarian language is a must.
Results and detail-oriented approach.
Understanding of clinical/medical data.
Good motivational, influencing, and coaching skills.
Ability to work on multiple projects and manage competing priorities.
In-depth therapeutic and protocol knowledge.
Strong organizational and problem-solving skills.
Effective presentation skills.
Ability to deliver results to appropriate quality and timeline metrics.
Ability to work across cultures and geographies with high awareness of cultural differences.

Nice to Have

Experience in the clinical research field is preferred.

Team & Environment

You will collaborate closely with project resources, including CRAs, CTAs, and the Centralized Monitoring team. You’ll support CMS leads and provide mentorship to Associate Central Monitors, operating within a global team structure.