Clinical Research Associate II - IQVIA Biotech - Belgium - Home Based (m/w/d)

Location: Home based, but candidates must be based in Belgium

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Participate in the preparation and execution of Phase I-IV clinical trials.
• Conduct site evaluation, initiation, interim close-out, field evaluation, and on-site monitoring visits.
• Coordinate investigator sites and internal departments, provide study training, and support investigator meetings.
• Review electronic CRF data and source documentation, resolve data queries, and ensure clinical data quality and integrity.
• Prepare monitoring reports and correspondence while ensuring study deliverables meet required timelines.
• Mentor junior CRAs and support field training for CRAs and other clinical research staff.

Requirements

• At least 1-2 years of on-site clinical monitoring experience.
• Strong knowledge of clinical research processes, medical terminology, and all functional areas of clinical trials.
• Knowledge of current GCP/ICH guidelines applicable to clinical research.
• Ability to manage multiple complex trials, prioritize independently, and work effectively in a matrix environment.
• Strong Dutch and English communication skills required.
• Ability to build productive relationships with study personnel, healthcare professionals, and cross-functional teams.

Nice to have

• French communication skills.

Culture & Benefits

• Home-based work arrangement within Belgium.
• Fast-paced environment focused on smaller biotech and emerging biopharma clients.
• Opportunity to contribute to clinical studies involving innovative therapies for unmet medical needs.
• Collaboration with global clinical monitoring, clinical management, and oversight teams.