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
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
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a (Senior) Clinical Research Associate in our client dedicated FSP team - Belgium – Make an Impact at the Forefront of Innovation We have successfully supported the
Senior Clinical Trial Associate Department: Clinical Development Employment Type: Permanent - Full Time Location: Agomab Antwerp Description The Senior Clinical Trial Associate (CTA) is providing high-quality administrative and operational support to the Clinical Operations Team. In this role, you will
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
Change people’s lives and love what you do! Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market-leader in implantable hearing devices, more people choose a Cochlear-branded cochlear
Locations: Leuven, Belgium Categories: Clinical Monitoring Req ID: 12993 Looking for the next step in your career? Medpace is hosting a virtual event specifically for Clinical Research Coordinators / Study Nurses who aspire to become Clinical Research Associates: Take
Position Summary: The Senior Manager, Clinical Operations – Clinical Process Owner is responsible for leading the governance, harmonization, and continuous improvement of Clinical Operations processes across the organization. The role owns the development, simplification, alignment, and lifecycle management of
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
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
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
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources
Make your mark for patients We are looking for a GMP Process and Operations Compliance Lead who is collaborative, quality‑driven, and proactive to join our Clinical Manufacturing team (Pharma and Biologicals, mAb and Gene Therapy), based in
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