
Study Start-Up Clinical Research Associate, FSP Belgium at IQVIA
About the role
SSU Clinical Research Associate
- IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team CRA (Junior
- Senior) . At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.
Your responsibilities will include:
- Conduct site selection, initiation, monitoring, and close‑out visits
- Manage study start‑up activities up to site green light
- Ensure compliance with ICH‑GCP, regulatory requirements, and SOPs
- Track study progress (regulatory submissions, recruitment, data quality)
- Collaborate closely with investigative sites, clients, and internal teams
- Support seamless handover to execution CRAs
Your Profile
- University degree in scientific discipline or health care
- Experience in Pharma Industry, and/or Clinical Trials environment
- Very good computer skills including MS Office
- Excellent command of Dutch, French and English language. Belgium based.
- Organizational, time management and problem-solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Flexibility to travel
- Driver’s license class B
What you can expect:
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Excellent working environment in a stabile, international, reputable company
- Company car, mobile phone and attractive benefits packaging
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Required skills
Clinical research
Site monitoring
GCP
Documentation
Communication
About IQVIA
Zaventem
Headquarters