clinical study

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...

Questa posizione è in IQVIAIl processo di selezione sarà interamente gestito IQVIA.Questa opportunità è disponibile in Reading - United Kingdom, Belgrade - Serbia, Rome - Italy, Paris - France, Vienna - Austria, Budapest - Hungary, Amsterdam - Netherlands, Dublin - Ireland, Sofia - Bulgaria, Frankfurt - Germany, Athens - Greece, Ljubljana – Dunajska -...

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,...

IQVIA is seeking a senior Biostatistician to lead the statistics for a clinical program. You will define statistical strategy, oversee study design and data analyses, and ensure regulatory submissions are robust. The role requires 8+ years in clinical trial statistics, expertise in SAS/R, and experience with Bayesian methods and adaptive designs....

Amaris Consulting is recruiting a Senior Clinical Research Associate to manage clinical activities in cardiac electrophysiology across multiple sites. You will oversee site performance, ensure data quality, and liaise between the study team and site personnel.You will ensure patient safety, support trial execution, and comply with SOPs and regulatory...

Actalent seeks a Senior Clinical Research Associate to oversee clinical study activities within a MedTech environment. The role involves monitoring sites, ensuring data quality, and maintaining regulatory compliance across projects.The ideal candidate has a Life Sciences degree, at least 4 years of CRA site-monitoring experience, and proficiency in GCP....

Overview We are seeking a Hematologist - Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a...

IQVIA is seeking a senior Biostatistician to lead the statistics for a clinical program. You will define statistical strategy, oversee study design and data analyses, and ensure regulatory submissions are robust.The role requires 8+ years in clinical trial statistics, expertise in SAS/R, and experience with Bayesian methods and adaptive designs....

DermatologyWe are seeking several Medical Directors to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a...

Dermatology We are seeking several Medical Directors to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a...

ResponsibilitiesMake sure to apply with all the requested information, as laid out in the job overview below.(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...

Overview Our clinical operations activities are growing rapidly, and along with it our Supply Chain is growing more complex. We are currently seeking a full-time, Supply Chain Specialist to join our Clinical Operations team. This position partners with cross functional teams to identify the right vendors and products that will meet the needs of a given...

PSI is a global Contract Research Organization (CRO) with over 30 years of experience supporting clinical research around the world. We combine the stability of an established organization with the agility and innovation needed to advance modern clinical trials. Guided by a commitment to quality and on-time delivery, we partner with clients across a broad...

Alimentiv is seeking an experienced CRA to independently perform, coordinate and oversee site monitoring activities across clinical studies. The role ensures protocol and regulatory compliance and acts as a liaison between sponsor, Alimentiv, and investigative sites.The position involves mentoring CRA I and II, participating in audits, and aiding with site...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of...

PSI is a leading Contract Research Organisation seeking a Senior Freelance Clinical Research Associate in Belgium. You will lead onsite monitoring visits, review CRFs, and ensure data quality while maintaining strong site relationships and study timelines.Fluency in Dutch and English, proficiency in French, and willingness to travel are required, along with...

Don't see an opening that quite matches what you're looking for, or not ready to make a move yet? Let us know! We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the Process Looks Like A Talent Acquisition...

Exciting opportunity with a global biotech organisation seeking an experienced Biomarker Data Science leader to help shape how biomarker data drives clinical development decisions.This is a highly strategic role where you'll work across translational research and clinical development, ensuring biomarker insights influence study design, development strategy,...

Senior Clinical Research Associate, Belgium, Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers,...

IMPORTANT: after you apply, please check your email. We send you a link to complete your application — it is not considered until that last step is done. If you do not see it, check your spam folder.This is a fully remote position, open to candidates based in Belgium.Pay: $30–$60/hrRole Title: Medical Writer (Pharmaceutical)Role Type: ContractorLocation:...