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 successful execution
Clinical Research Associate (CRA) - Belgium Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our
Clinical Research Associate Belgium - Single Sponsor Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping
Locations: Belgium Categories: Clinical Research Associate Req ID: 12184 Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical / Country Operations team in Belgium. This position will work on
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 while making
Locations: Leuven, Belgium Categories: Clinical Research Associate Req ID: 12182 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 while making
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
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 Study Associate
The Clinical Research Regulatory Coordinator is responsible (primarily or in supporting role) for all activities related to the submissions of clinical trials applications in the CTR online platform known as Clinical Trial Information System (CTIS). The submitted CTA comprises
What Youll Do: 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
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
Please note that this is a ‘internal job posting’ link, intended for GSK/ViiV employees only. Contingent Workers should check with the recruiter of the Job Requisition to confirm whether the job is open to contingent workers
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
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
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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description SUMMARY The Senior Application Administrator is responsible for the administration, configuration, validation, and lifecycle management of laboratory middleware and instrument interfaces within a regulated GxP environment. This role serves
Laboratory Technician II, Genomics Services We are actively looking for a motivated and experienced Laboratory Technician II to join our Genomics Unit. In this role, you will play a crucial part in our cutting-edge laboratory, performing
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Regulatory Affairs Manager – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750