10.06.2024 | Full-time | ParexelActivities and deliverables of one or more External Relationship Management specifics about this advertised role100% Home-basedProvide management and matrix management to the wider vendor teamA focus on Vendor GovernanceGeneral oversight of the functionManagement of the study portfolioReviewing
Uita-te mai târziu10.06.2024 | Full-time | GfKstudies to ensure all involved parties understand timelines, responsibilities, and study ort research project teams by leveraging relationships with overseas suppliers to facilitate communications, trouble-shooting and issue resolution. Coordinate operational aspects of projects
Uita-te mai târziu10.06.2024 | Full-time | IQVIAOf clinical trials at a country level in accordance with ICH-GCP and other applicable local ONSIBILITIES OVERVIEWPartner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery. (Accountable for study
Uita-te mai târziu10.06.2024 | Full-time | LeverXAnd SAP Fieldglass. You will have a chance to take effective educational programs and study the technologies you have a lack of experience in. There is an opportunity to get certified in multiple application irements 5+ years of experience in the relevant rience in one or several SAP
Uita-te mai târziu10.06.2024 | Full-time | ContinentalOr Chemistry you are studying in one of these faculties and you want to use your theoretical knowledge to work for one of our projects, we offer you the opportunity of a paid summer practice of 6 up to 12 weeks, between July and ficăriEnrolled in bachelor's knowledge
Uita-te mai târziu10.06.2024 | Full-time | ParexelHungary, UK, Romania Croatia. This will be a home based role. Please note you must be fluent in main responsibility of the Site Contract Associate is the negotiation of study specific generic and country Clinical Site Agreement (CSA) templates with the Sponsor and support the PL
Uita-te mai târziu10.06.2024 | Full-time | Signant HealthProject Assistant for one of our Global Support Services teams in Iasi working on the Operations area of the business. The position gives you a great view on how a clinical study is being set up. The team is working on managing accesses needed by study personnel once a clinical study is live. Prior
Uita-te mai târziu10.06.2024 | Full-time | Lugoj | HELLATeamCoordinating all quality-relevant activities e.g. Risk Assessment to prepare the sourcing. Checking whether the manufacturing feasibility study is available and whether supplier locations and processes are releasedYOUR QUALIFICATIONSTechnical University degree in electrical or mechanic's mum 1 year
Uita-te mai târziu10.06.2024 | Full-time | Thermo Fisher ScientificCommunication skills, with the ability to communicate effectively with medical personnelManagement of the delivery of study suppliesStrong customer focusEffective interpersonal skillsStrong attention to detailEffective organizational and time management skillsProven flexibility and adaptabilityAbility to work
Uita-te mai târziu10.06.2024 | Full-time | Parexel& ResponsibilitiesDevelop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual ss change controls and provide regulatory assessments of quality changes in production and quality ew study reports from the quality control
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