Associate Centralized Monitor, Dutch Speaking, South Africa - Bloemfontein at IQVIA

Job Summary


Provide project and study support to clinical teams by performing centralized monitoring, administrative tasks, data review, and system updates. Ensure all work aligns with SOPs, ICH-GCP, regulatory requirements, and project timelines.


Key Responsibilities


Complete required role training and follow all SOPs and quality standards.
Provide administrative support (run reports, maintain trackers, prepare status updates, follow up on outstanding items).
Update and maintain study systems and support compliance with project timelines.
Assist in preparing i-Site Packs and other study documents.
Perform centralized monitoring activities and assess site/data quality.
Monitor site performance metrics and follow up on missing data, queries, SDV backlog, and visit schedules.
Identify site-level risks and recommend/track corrective actions.
Conduct Subject Level Data Review (SLDR) and escalate issues as needed.
Perform study-specific analytics and support trend analysis.
Handle access management tasks and coordinate with vendors where required.
Act as backup for Centralized Monitors/Senior Centralized Monitors.
Support technical tools (Excel formulas, macros, tool design) as needed.
Maintain effective communication with sites, CRAs, and internal teams.


Qualifications


Bachelor's/Postgraduate degree in Life Sciences or related field.
At least 1 year in clinical research or centralized monitoring preferred.
Fluent in Dutch
Proficient with MS Office, especially Excel.
Strong communication, organization, and problem-solving skills.
High attention to detail, accuracy, and data quality.
Ability to work effectively with cross-functional teams and external sites.