28.06.2024 | Full-time | IQVIAInitiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.• Administer protocol and related study training to assigned sites
Uita-te mai târziu28.06.2024 | Full-time | PSIJob DescriptionThe Milestone One Site Coordinator role supports Clinical Study Sites in clinical trial related activities according to ICH-GCP, local regulations, protocol requirements within Study specific defined timelines and enrollment function of the role may include, but not limited
Uita-te mai târziu28.06.2024 | Full-time | ProPharma GroupRCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D
Uita-te mai târziu28.06.2024 | Full-time | KauflandDe personal Colaborezi cu autoritățile și clinicile de medicina muncii pentru efectuarea analizelor și a controalelor medicale periodice Monitorizezi absențele și timpul de lucru, identifici erorile de pontare și efectuezi corecturile de timp în sistemul de înregistrare a timpului de lucru În cazul
Uita-te mai târziu28.06.2024 | Full-time | Antal InternationalAnd maintain direct contact with hospitals and clinics in Romania. Develop and nurture relationships with customers, providing tailored solutions and high-quality support to meet their needs effectively. Market Analysis and Strategy Continuously monitor the market and competitors' activities to identify
Uita-te mai târziu28.06.2024 | Full-time | IQVIAJob OverviewThe Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of a program of assigned clinical supply chain projects. The Clinical Supply Chain Manager will support the ongoing development and optimization of the Clinical Trial Supplies department
Uita-te mai târziu28.06.2024 | Full-time | IQVIAClinical Research AssociateIQVIA Bucharest is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety
Uita-te mai târziu27.06.2024 | Full-time | PSIJob DescriptionAs a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the willConduct and report SSV, SIV, RMV, COV onsite monitoring
Uita-te mai târziu27.06.2024 | Full-time | Worldwide Clinical TrialsRequisition Number 7966 Position Title Manager, Data Safety & Monitoring Board (DSMB) External Description Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create
Uita-te mai târziu27.06.2024 | Full-time | Mindray IndiaThe regional teams for all monitoring related enquiries, and to deliver training where necessary. This position requires frequent interaction with head-quarters, marketingclinical marketing ,sales, partnerscustomers, and other cross-functional team members. Travel within Europe is also a requirement
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