clinical study

Fulltime - International - Strategy / Senior Leadership YOUR MISSION - What you’ll achieve You’ll take ownership of how XEOS demonstrates and translates the clinical, economic, and operational value of our disruptive specimen PET-CT platform. You’ll develop a coherent global market access and value strategy that supports hospital adoption and...

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...

## Medical Affairs and Evidence Generation Asset Lead –Executive DirectorApply:Belgium - Remote:Switzerland - Remote:Full time:Posted Today:REQ-4573*Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline...

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,...

PURPOSE OF THE FUNCTIONThe Statistical Modeling and Innovative Solutions team partners with colleagues across Quantitative Sciences and other cross-functional teams to develop and apply innovative approaches to optimize study designs and clinical development plans, strengthen data‑driven decisions, and support evidence and insights generation across the...

argenx is seeking a senior statistician to lead the development and implementation of innovative study designs in clinical trials, including adaptive designs and Bayesian approaches. You will pilot AI/ML solutions for disease modeling and collaborate across Quantitative Sciences to translate evidence into data-driven decisions.Applicants should hold a PhD in...

Planet Pharma are currently partnered with an exciting global biotech and we are actively seeking an experienced Global Medical Safety Lead to join the business on a permanent basis. This is a hybrid role. Key Responsibilities: - Act as the medical safety lead for assigned products, providing strategic pharmacovigilance and benefit-risk expertise across...

Planet Pharma are currently partnered with an exciting global biotech and we are actively seeking an experienced Global Medical Safety Lead to join the business on a permanent basis. This is a hybrid role. Key Responsibilities: - Act as the medical safety lead for assigned products, providing strategic pharmacovigilance and benefit-risk expertise across...

Planet Pharma are currently partnered with an exciting global biotech and we are actively seeking an experienced Global Medical Safety Lead to join the business on a permanent basis. This is a hybrid role. Key Responsibilities: - Act as the medical safety lead for assigned products, providing strategic pharmacovigilance and benefit-risk expertise across...

Planet Pharma are currently partnered with an exciting global biotech and we are actively seeking an experienced Global Medical Safety Lead to join the business on a permanent basis. This is a hybrid role. Key Responsibilities: - Act as the medical safety lead for assigned products, providing strategic pharmacovigilance and benefit-risk expertise across...

I'm supporting a major biopharmaceutical company that is building out its Quantitative Clinical Pharmacology capability and looking for an experienced Pharmacometrics Lead. This is a strategic role for someone eager to push the boundaries of model‐informed drug development. This position is perfect for someone who thrives at the intersection of advanced...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

Brief DescriptionThe Backend Software Engineer is responsible for the following:Develop and/or maintain high expertise in software engineering and best practices with anemphasis on Python and Django.Develop safe and efficient custom solutions to complex clinical trial data/workflowproblems.Program and configure study-specific reports.Work with clients and...

AL Solutions is seeking a Senior Clinical Research Associate to lead set-up, execution and oversight of Phase I–IV trials across Belgium with occasional travel in the Benelux region. You will monitor studies to ensure compliance with ICH-GCP, EU and local regulations, study protocols, and SOPs, while mentoring junior team members.The role involves start-up...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

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:...