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The Clinical Operations Development Lead (CODL) is a key member of the Indication Development Team (IDT), overseeing clinical activities for a specific therapeutic indication (CODL) or across all indications for an asset (early/late phase CODL). The CODL provides operational input and drives strategy for clinical development across the lifecycle of an asset,...

argenx is seeking an experienced Project Toxicologist with expertise in the nonclinical development of multiple drug modalities, particularly with large molecules. Five or more years of relevant experience in cross-functional project teams is preferred.Project toxicologists at argenx support the development of our compounds from an early stage (lead...

The Franchise Clinical Operations Development Lead (CODL) is responsible for the strategizing, planning, leading and execution of the operational path for all indications within a franchise from first in human studies through authorization and commercialization. The franchise may involve several assets and/or may cover specific development phases across all...

IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. IQVIA Biotech has an exciting position within its EU Clinical Monitoring team. The Clinical Monitoring...

At Ardena, we’re helping shape the future of medicine. Our teams work on the development of innovative and complex therapies that can improve the lives of patients around the world. As a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO), Ardena partners with pharmaceutical and biotech companies to...

Clinical monitoring At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and IB updates, Biomarker Reports, and...

We are looking for a strategic, collaborative and solutions-oriented QA Expert to join our Quality Assurance team within Braine Internal Manufacturing, based at our UCB campus located in Braine-l’Alleud, Belgium. About The Role As QA Expert, Analytical Services, you will provide leadership, governance and accountability across the analytical and laboratory...

# Senior Manager Clinical OperationsBeerse, Belgium Full timeClinical Development ManagerNotify me about similar jobsView Full Job & Apply at Johnson & JohnsonJohnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this...

Senior Director, Therapeutic Area (Oncology/Hematology) Company: ICON plcJob Title: Senior Director, Therapeutic Area – Oncology/HematologyLocations: Blue Bell, Pennsylvania, USA (Remote) Mechelen, Belgium Reading, United Kingdom Job Type: Full-TimeWork Mode: Remote / HybridIndustry: Clinical Research / Oncology / Pharmaceutical / CROExperience Required:...

IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment.The sector we are in is cutting edge for therapies with un-met medical need. IQVIA Biotech has an exciting position within its EU Clinical Monitoring team. The Clinical Monitoring...

Clinical Research Associate IQVIA Belgium is looking for talented and motivated CRA to join our Site Management team. 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. Perform...

Join to apply for the Clinical Operations Development Lead role at argenx The Clinical Operations Development Lead (CODL) is a key member of the Indication Development Team (IDT), overseeing clinical activities for a specific therapeutic indication (CODL) or across all indications for an asset (early/late phase CODL). The CODL provides operational input and...

Regulatory Affairs Specialist - Belgian Dutch speaker (Western Europe) page is loaded## Regulatory Affairs Specialist - Belgian Dutch speaker (Western Europe)remote type: Remotelocations: Virtual Belgium: Virtual Netherlands: Virtual Francetime type: Full timeposted on: Posted Yesterdayjob requisition id: JR102472**Who we are**We're a global, midsize CRO...

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...

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...

Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study...

Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study...

Wir suchen aktuell: Schichtleiter Logistik (m/w/d) in Landsberg Sind Sie auf der Suche nach einer neuen beruflichen Aufgabe? Gerne begleite ich Sie auf dem Weg dahin!Zum nächstmöglichen Zeitpunkt suche ich stellvertretend für mein Kundenunternehmen aus der Logistikbranche, einen Schichtleiter Logistik (m/w/d) zur...

At Ardena, we’re helping shape the future of medicine. Our teams work on the development of innovative and complex therapies that can improve the lives of patients around the world. As a global Contract Development and Manufacturing Organization (CDMO) and Contract Research Organization (CRO), Ardena partners with pharmaceutical and biotech companies to...