Vacatures 1 tot 10 van 36
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Oxford Global Resources - Haarlem
pharmaceutical industry or a Contract Research Organization (CRO). In-depth understanding of drug development processes, clinical trial management, and regulatory requirements for Phase II and III studies. Proven experience working with- Volledige vacature bekijken
Principal Medical Writer (remote) Life Sciences)
Yacht - Utrecht
following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical regulatory documents across multiple therapeutic areas as assigned- Volledige vacature bekijken
Oxford Global Resources - Leiden
crucial role within the European Quality Control team, working closely with laboratory professionals to ensure the highest standards in clinical trial support and quality management. This position involves providing expert QC- Volledige vacature bekijken
Assistant Professor in Biostatistics
Erasmus MC via Talent - Rotterdam
research questions. The members of the department lead research lines in joint models for longitudinal and time-to-event data, (dynamic) prediction models, clinical trial methodology, models for rare diseases, growth curve models- Opslaan
Professor in Causal Decision-making for Clinical stu...
Ghent University via Academic Positions
03/11/2024 (DD/MM/YYYY) 23:59 (Brussels time) → Discipline: Causal Decision-making for Clinical studies → 10% Assistant professor → Faculty of Sciences → Reference number: 202409/WE/ZAP/004 ABOUT GHENT25 dagen geleden - Preview - Opslaan
Study Start Up Associate I - Dutch Speaker
Icon Plc - Utrecht
innovative treatments and therapies. What You Will Be Doing: Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency- Preview - Opslaan
Study Start Up Associate I - Dutch Speaker
Icon Plc - Utrecht
regulatory requirements, and contributing to the advancement of innovative treatments and therapies. What You Will Be Doing: Assisting in the preparation and submission of regulatory documents, such as clinical trial - Preview - Opslaan
Pra via Talent - Utrecht
degree in a life science• At least 12 months of a CTA/ Clinical Trial Assistant or similar role experience within the clinical /pharmaceutical industry• Understanding of ICH GCP Compliance• Excellent communication and organizational- Opslaan
PRA via Jobsonline - Utrecht
patient confidentiality Other duties as assigned You will need: Minimum Bachelor's degree in a life science At least 12 months of a CTA/ Clinical Trial Assistant or similar role experience within the clinical - Preview - Opslaan
Icon Plc - Utrecht
drive and fly) Maintain Sponsor and patient confidentiality Other duties as assigned You will need: Minimum Bachelor's degree in a life science At least 12 months of a CTA/ Clinical Trial Assistant or- Preview - Opslaan
Vacatures, Stoevelaar - Amsterdam
arbeidsvoorwaarden, architect, area, arts, afgestudeerden, areamanager, artsen, banen, assessment, artsenbezoekers, assistant , fysiotherapeuten, artsenorganisaties, assistent, biomedisch, bewegingswetenschappers, associate, assistenten- Opslaan
Corsano - The Hague
great fit for this role to info@corsano.com. Please include "Customer Service Speciailist" in the subject line. Clinical Assistant Corsano Health is op zoek naar een enthousiaste Clinical Assistent die per 1 augustus kan- Preview - Opslaan
Disease mechanisms and new therapies background info...
Radboudumc - Rha
organoids) Clinical trial facilities including outcome measures and support Develop methods to investigate the implementation of person-centered therapies. These include statistics in small groups or n=1 trials as well as- Opslaan