clinical study

IQVIA Belgium is seeking a Junior Clinical Research Associate to join our sponsor-dedicated team. You will gain experience across therapeutic areas and build a strong career within IQVIA.Your responsibilities include site visits, regulatory compliance assessments, tracking submissions and data queries, and collaborating with study sites and clients. Fluency...

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...

Step into research at the Pfizer Clinical Research Unit (PCRU) – Brussels Are you passionate about patient care, detail-oriented, curious and adaptable in a dynamic environment? Do you thrive on learning and driving innovation? If so, this could be your next chapter in the world of clinical research. As a clinical research nurse, you will work closely...

Doctoral fellow - Department of Experimental Clinical and Health Psychology Department: PP05 - Department of Experimental Clinical and Health Psychology Degree: Master’s degree in Psychology or another relevant Master’s degree Occupancy rate: 100% Vacancy type: Research staff YOUR TASKS As a PhD student, you will join our team and conduct research within...

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan...

A global Clinical Research Organization is seeking a Start up Specialist to work remotely in Belgium. The ideal candidate should have a bachelor's degree in life-science and at least 1.5 years of experience in Ethics Committee and Competent Authority submissions within a CRO, Pharma, or Biotech. Responsibilities include managing submissions, keeping abreast...

Step into research at the Pfizer Clinical Research Unit (PCRU) – BrusselsApply fast, check the full description by scrolling below to find out the full requirements for this role.Are you passionate about patient care, detail-oriented, curious and adaptable in a dynamic environment? Do you thrive on learning and driving innovation? If so, this could be your...

Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical development plans, collaborate with cross-functional team...

We are looking for a Clinical Supply Compliance Process & Governance Lead who is quality-minded, collaborative, and improvement-driven to join our Clinical Supply Chain team, based at our UCB campus located in Braine-l'Alleud, Walloon Brabant, Belgium. About the role You will play a key role in ensuring that Clinical Supply Chain processes meet GMP,...

Reading, Berkshire, United Kingdom Belgrade, Serbia Paris, France Warsaw, Poland Amsterdam, Netherlands Madrid, Spain Budapest, Hungary Dublin, Ireland Frankfurt, Hesse, Germany Ljubljana – Dunajska, Slovenia Bucuresti, Romania Brussels, Brussels-Capital Region, Belgium Gothenburg, Sweden Copenhagen, Denmark Bratislava, Slovakia Full time R1503450 Lead...

Reading, Berkshire, United KingdomBelgrade, SerbiaParis, FranceWarsaw, PolandAmsterdam, NetherlandsMadrid, SpainBudapest, HungaryDublin, IrelandFrankfurt, Hesse, GermanyLjubljana – Dunajska, SloveniaBucuresti, RomaniaBrussels, Brussels-Capital Region, BelgiumGothenburg, SwedenCopenhagen, DenmarkBratislava, SlovakiaFull timeR1503450Lead full scope of...

AbbVie in Belgium is seeking a Clinical Research Associate (CRA) to support clinical studies across Belgium. The role partners with investigators and site teams to promote study delivery, data quality, compliance and a positive site experience.The CRA will conduct site evaluation, initiation, monitoring and close-out activities, ensure patient safety,...

Organisation/Company Université catholique de Louvain Research Field Medical sciences » Other Psychological sciences » Psychology Psychological sciences » Other Researcher Profile Established Researcher (R3) Application Deadline 5 Nov 2026 - 11:00 (UTC) Country Belgium Type of Contract Temporary Job Status Full-time Is the job funded through the EU...

Arcadis is seeking an experienced Senior Clinical Research Associate to support and monitor clinical studies within a MedTech environment. You will manage multiple study sites, ensure protocol and GCP compliance, and drive data quality and study performance.Applicants should have 4+ years of site monitoring experience, strong communication skills, and...

Labcorp is seeking a remote Study Design Lead to join our Central Labs Services team in Belgium. You will interpret sponsor protocol requirements, design comprehensive databases, and advise on study design choices in collaboration with the Global Study Manager.You will coordinate internal feasibility, contracts, and supply forecasting while maintaining...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...

Responsibilities(a) Site managementStudy site selection, initiation (SIV) and clinical monitoring.Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.Prepare and conduct SIV to ensure adequate study training for relevant site staff to...