Ervaren Monitor Klinische Studies
Location: Zaventem, Belgium
R1350084
Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.
As a Clinical Research Associate within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic
area and work with cutting-edge technology developed specifically for CRAs by CRAs. With access to world-class training and professional
development, we’ll give you the tools you need to create the career you want.
- Full Time
- Level: Entry-level, Mid-level, Senior-level
- Travel: Yes
Success profile
What makes CRAs aligned to our full-service model successful? Check out the top traits we're looking for and see if you have the right mix.
- ANALYTICAL
- ORGANIZED
- COMMUNICATOR
- PROBLEM-SOLVER
- FACILITATOR
- VERSATILE
Explore this
career path
As you grow your CRA career at IQVIA, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.
-
CRA 1
-
CRA 2
-
Senior
CRA 1 -
Senior
CRA 2 -
Senior
CRA 3
Quote
“IQVIA empowers you to drive your own path within the organization. As no person’s route is the same and the clinical research landscape is forever changing, you are encouraged to continually seek career growth opportunities and to align your interests with your career goals.”
Lauren, Senior Clinical Research Associate 2
“I really enjoy the diversity of teams and clients the CRA role provides, in addition to the ability to speak with so many different key opinion leaders across the country. Progressing through to a Senior CRA, and now acting as Lead CRA for one of our largest gastroenterology studies, I'm excited at the continued opportunities for success and growth in clinical leadership.”
Joseph, Senior Clinical Research Associate 2
“I work with the most incredible brave minds. We share energy and passion to bring new medicines to the market.”
Carolina, Senior Director, R&D Solutions
What you
can expect
-
Professional Development
Resources that promote your career growth
-
Work-Life Balance
Leaders that support flexible work schedules
-
Best-in-class Training
Programs to help you build your therapeutic knowledge
-
Variety
Dynamic work environments that expose you to new experiences
-
Growth Potential
Clear pathways to success
-
Therapeutically Aligned
Protocols aligned to your expertise
Ervaren Monitor Klinische Studies
Job description
ERVAREN CRA/MONITOR KLINISCHE STUDIES
WAT WIJ ZOEKEN
- MSc en/of BSc opleidingsniveau.
- Kennis van Nederlands, Engels en Frans.
- Goede kennis en toepassing ICH-GCP.
- Minimaal 2 jaar ervaring als CRA.
- Ervaring in het gebruik van CTMS, eTMF en EDC systemen.
- Ervaring in verschillende studies, fases, visites en therapeutische indicaties.
- Passie voor wetenschap, helpen van patiënten en samenwerken met de sites.
FUNCTIEOMSCHRIJVING
- Uitvoeren van visites (zoals selectie, initiatie, monitoring en close-out) volgens ICH-GCP richtlijnen.
- Begeleiding van junior CRAs.
- Ondersteuning van de site(s) i.v.m. patiëntenwerving.
- RCA en CAPA management.
- Rapportering van visites en voortgang van de studies.
- Beheer en archivering van studie-documenten in eTMF.
- Samenwerking met het project-/studie team.
- Documentatie in Monitoring Visit Reports en follow-up brieven.
#CRAFSAJD
#LI-ANAHDEZCIP
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
Join our Global Talent Network
Let’s stay connected. Join our Global Talent Network to receive alerts when new opportunities become available that match your career ambitions.
Join our network