03.07.2024 | Full-time | AL SolutionsTaylor Young has partnered with a Global CRO looking for an experienced Clinical Research Associate to expand their highly knowledgeable Clinical operations team Romania. This an incredible and exciting opportunity to join a leading international organization that specialises in multiple
Uita-te mai târziu01.07.2024 | Full-time | IQVIAmonitoring and close out visits in accordance with contracted scope of work, using good clinical practices applicable regulations, SOPs and work instructionsComplete appropriate therapeutic, protocol and clinical research training to perform job duties. Work collaboratively with other functional groups
Uita-te mai târziu01.07.2024 | Full-time | IQVIATo continued growth, we are seeking new brave minds to join our award winning and innovative viewUnder the direction and guidance of the Real-World Late Phase Research Clinical Operations Lead, Line Manager or Project Manager, conduct clinical remote monitoring visits and other clinical research
Uita-te mai târziu01.07.2024 | Full-time | CPS Fortrea Clinical Development Limited, Maidenhead Sucursala BucurestiOperations and clinical trial teamResponsible for project management of the assigned studies actively plans, drive and track execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment, execution and close outReview Monitoring
Uita-te mai târziu29.06.2024 | Full-time | IQVIAJoin us in our exciting journey!!IQVIA is looking for a Clinical Research Associate to the multisponsor would be responsible forPerforming visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP ort of the site(s) i.v.m. patient
Uita-te mai târziu28.06.2024 | Full-time | IQVIAJob OverviewPlan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations
Uita-te mai târziu28.06.2024 | Full-time | Orange Business ServicesTa cu un abonament gratuit la o clinică medicală privată.Dacă vrei să-ți împrospătezi starea personală, avem tot felul de programe de Wellbeing pentru zen-ul tău, iar dacă te interesează dezvoltarea profesională, află că ai ajuns exact unde îți doreai îți oferim training-uri dintre cele mai variate, consiliere
Uita-te mai târziu28.06.2024 | Full-time | CPS Fortrea Clinical Development Limited, Maidenhead Sucursala BucurestiDegree or equivalent in relevant health care ired experience and skills+ A minimum of 6 years of relevant experience in clinical research including direct field monitoring experience or management/oversight of such individuals, with a demonstrated record of accomplishments. Experience
Uita-te mai târziu28.06.2024 | Full-time | IQVIAInitiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging
Uita-te mai târziu28.06.2024 | Full-time | IQVIAParticipants like ECG, BPM, Glucose Monitoring etc. This role will be responsible for business requirement understanding review, test case authoring and UAT executionResponsible for creating site and subject facing documentation like Investigator Manuals, Patient Facing Guides, Site reference guidesResponsible
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