27.06.2024 | Full-time | ProclinicalFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-onsibilitiesTravel to sites to carry out site selection, initiation, monitoring and close-ort the development of a subject recruitment uate the quality and integrity of site
Uita-te mai târziu27.06.2024 | Full-time | Aspen MedicalAspen Medical seeks expressions of interest from experienced and qualified midwife nurses to join our team in supporting an oil and gas project in Libya. As a midwife nurse, you will be responsible for providing high-quality healthcare services in hospital or clinical settings. Contract Details
Uita-te mai târziu27.06.2024 | Full-time | ProclinicalFor clinical studies in phases I - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities will includeConduct a variety of different site visits. This is inclusive of selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment
Uita-te mai târziu27.06.2024 | Full-time | Thermo Fisher ScientificOur global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs
Uita-te mai târziu27.06.2024 | Full-time | PSIJob DescriptionAs a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators
Uita-te mai târziu27.06.2024 | Full-time | ParexelWhen our values align, there's no limit to what we can achieve. Job PurposeReporting to the Vendor Category Expert, the Vendor Startup Manager is responsible to provide technical expertise for the category throughout startup to close out to the VCE and indirectly to the Clinical Trial
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
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 | AL SolutionsIn the clinical research industry. They really encourage career progression and prioritise work life balance. Requirements - Life science degree educated - Independent on-site monitoring experience - 3 Years minimum as a CRA - Have in depth GCP knowledge Benefits - Excellent salary and benefits package - Career
Uita-te mai târziu27.06.2024 | 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
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