Clinical Research Associate II
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Motivated Clinical Research Associate II – Belgium
IQVIA Belgium is seeking a motivated Clinical Research Associate II practitioner to join our unique and dynamic sponsor dedicated model.
Role Overview
This role is based in Belgium.
Your Role
- Perform site monitoring visits (selection, initiation, monitoring and close‑out) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
- Administer protocol and related study training to assigned sites and establish regular lines of communication to manage ongoing project expectations and issues
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations, escalating quality issues as appropriate
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution; may support start‑up phase
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation
- Collaborate and liaise with study team members for project execution support as appropriate
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per‑site basis
Your Profile
- University degree in a scientific discipline or health care
- Minimum of 18 months of independent, on‑site monitoring experience as a CRA within a CRO or pharmaceutical environment
- Excellent communication skills in Dutch, French, and English, both written and spoken
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (GCP and ICH guidelines), organizational and problem‑solving skills
- Exceptional interpersonal and cross‑cultural communication skills to build strong trusted partnerships with Belgium site investigators and medical staff
- A collaborative mindset to work effectively with cross‑functional global teams, project managers, and local study coordinators
Why join us?
- Grow your career with access to development resources, training, and advancement opportunities
- Enjoy the flexibility and trust to balance your professional and personal commitments
- Expand your therapeutic knowledge through dedicated learning and development programs
- Be part of a successful global organization with an excellent reputation and supportive culture
- Benefit from a company car, mobile phone, and an attractive rewards and benefits package
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