Locations: Leuven, Belgium Categories: Clinical Research Associate Req ID: 12510 The Entry Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision, compliance, and process efficiency? We are looking for an energetic Clinical Study Specialist I to join our growing Clinical Operations team and support the
Clinical Study Associate I Are you passionate about clinical research and interested in contributing to work that improves human health? If so, this opportunity may be a great fit for you. CellCarta is seeking an entry-level Clinical
About the Role Are you passionate about healthcare innovation and curious about how new ideas become real-world improvements for patients and healthcare professionals? The Clinical Study Unit (CSU) Belgium, part of Sanofis North Europe MCO, is looking
Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology
Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology
Assay Development Scientist - Genomics Services (Hybrid) Are you a scientist with expertise in molecular genetics and genomics technologies? Join CellCartas Genomics Services team as an Assay Development Scientist and contribute to the advancement of innovative
Job Description As a Lab Analyst working in pharmaceutical sciences, you will be responsible to perform analytical testing work, running existing methods and protocolsfocused on Solid-State Characterization Methods to cover the following activities: Solid state characterization
Company Description Sia is a next-generation, global management consulting group. Founded in 1999, we were born digital. Today our strategy and management capabilities are augmented by data science, enhanced by creativity and driven by responsibility. We’re
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating
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
Superlinear is building Holon, an Enterprise Orchestration Platform for the physical economy. Large companies that move or make goods run every part of their operation on its own system. One decides what stock is needed, another
What will you do? As Category Manager – Temp Labour & CSE for the Business Unit Bpost, you will play a key role in shaping and executing the procurement strategy for your category. You will act
Company Description Coface protects companies and helps them make credit decisions to increase their turnover on the domestic and export markets. With more than 70 years of experience and the largest international network, Coface has become a
Scale: We’re growing fast: Our community of 133+ million registered users and 261.000 active partners across 20 countries, have together already saved 517+ million meals from going to waste - avoiding over 1.4 Million tonnes of
Make your mark for patients We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and collaborative to join our Real‑World Evidence (RWE) team, helping to shape evidence generation strategies
Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between
Our Position Help build the digital future of our production environment Have you recently graduated and are you looking to take your first steps in a role where IT, automation and production come together? Then this
Welcome to the BDO family, a worldwide consulting firm where you can bring your own personality to your job! We help organisations grow sustainably with our expertise in audit & assurance, tax & legal, advisory and
Welcome to the BDO family, a worldwide consulting firm where you can bring your own personality to your job! We help organisations grow sustainably with our expertise in audit & assurance, tax & legal, advisory and