Clinical Trial Medical Monitor: Patient Safety

Location SAINT LOUIS, MO 63110 Scheduled Hours 40 Position Summary This position will be housed in the Department of Radiology, in the clinical research group of Dr. Richard Wahl. Mallinckrodt Institute of Radiology’s clinical theranostics program provides personalized medical management through targeted radiopharmaceutical diagnosis and therapy. The...

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are looking for an experienced Patient Safety professional on a six month assignment. The successful candidate will contribute to...

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are looking for an experienced Patient Safety professional on a six month assignment. The successful candidate will contribute to...

Lieu de l'emploi1200 Woluwé-Saint-Lambert FonctionDirecteur du Clinical Trial Center Type de contratTemps plein - CDI Date de clôture des candidatures25/11/26 Directeur du Clinical Trial Center Woluwé-Saint-Lambert Cliniques Universitaires Saint-Luc asbl - Woluwé-Saint-Lambert Description de l’ASBL, institution Rejoignez un hôpital au cœur de...

Excelya is seeking a Patient Safety professional for a six-month assignment to contribute to clinical safety activities, signal detection and benefit-risk assessment for assigned products.The role involves reviewing safety data from trials and post-marketing sources, supporting signal detection and risk management, and collaborating with Regulatory, Medical...

We are looking for an Associate Director, Clinical Trial Devices to join us in our Global Regulatory Device Strategy team, based in our office in Belgium, Brussels. About the role The Associate Director, Clinical Trial Devices (Device Single Point of Contact, DSPOC) is accountable for end-to-end leadership, coordination, and oversight of all device-related...

Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research,...

Clinical Research Coordinator in TurnhoutWorking Hours: 8-10 hours per week Start Date: Immediately Duration: Approximately 9 monthsKey ResponsibilitiesPrescreening and Screening tasksReview charts from the site data baseMaintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and...