Clinical Research Associate II (Clinical Research)

Location: Home-based, candidates must be based in the Netherlands; role associated with Amsterdam.

Company

IQVIA Biotech is a division of IQVIA providing clinical research services for smaller biotech and emerging biopharma clients.

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 monitoring visits.
• Review source documentation, electronic CRF data, investigational product inventory, and clinical data quality.
• Coordinate with investigators, sites, internal departments, the Clinical Trial Manager, and Lead CRA.
• Prepare monitoring reports, correspondence, and study deliverables according to timelines and procedures.
• Attend investigator and study-related meetings and mentor or train junior CRAs.

Requirements

• Minimum 1-2 years of onsite clinical trial monitoring experience.
• Strong knowledge of the clinical research process, medical terminology, and all functional areas of clinical trials.
• Knowledge of current GCP/ICH guidelines and clinical research procedures.
• Ability to manage multiple complex trials, prioritize independently, and work effectively in a matrix environment.
• Strong Dutch and English communication skills required.
• Excellent communication, problem-solving, relationship-building, and clinical data review abilities.

Culture & Benefits

• Fast-paced environment focused on smaller biotech and emerging biopharma clients.
• Work with clinical studies developing therapies for unmet medical needs.
• Collaboration across clinical monitoring, clinical management, and oversight functions.
• Home-based work arrangement within the Netherlands.