Clinical Monitor Kanton Nidwalden Jobs

 ...Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking a: Clinical Operations Coordinator for a 12 months-contract based in Basel area. Main Responsibilities: ~Assisting the clinical... 

 ...support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes. Clinical Operations Manager SRS 5727 Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland,... 

 ...candidates in finding promising career opportunities and offer the latest in skill development training programmes. Event Manager Clinical Development 100% Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare... 

 ...candidates in finding promising career opportunities and offer the latest in skill development training programmes. Event Manager Clinical Development and Medical Affairs 80% Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in... 

 ...contract based in Kaiseraugst, Switzerland.   Background: The Clinical Distribution organization’s objective is to cost-effectively...  ...functions and performance (project support, UAT, system monitoring and housekeeping) ~Provide support and advanced knowledge for... 

 ...Programmer(s) for development for the allocated study(ies) ·Organizes, monitors and tracks the testing of data entry screens (eCRF layout),...  .... Makes sure processes are driven in collaboration with key Clinical Development (CD) stakeholders ·Generates study metrics and... 

 ...~Analyzes genomics data and contextualizes results to advance understanding of drug mechanism of action and pharmacodynamics in clinical trials and pre-clinical models. ~Mines and re-analyzes published and publicly available data to support genomics study design and... 

 ...support and interface with Brickwork Role Requirements: ~A valid working/residency permit or Swiss/EU-Citizenship is required ~Clinical Trial/Medical Affairs experience in a pharmaceutical company or a contract research organization is required. Would you like to... 

Hello, I'm Raquel, the co-owner of Phoenix Adventure, a camp company for children aged 3 to 17 years. At Phoenix Adventure, we run creative, fun, and full of surprises camps. We create a fantasy world for children to spend their holidays playing and enjoying nature. ...

 ...approve deviations and CAPAs. ~Provide guidance on the resolution of testing issues, discrepancies and Out of Specifications (OOS). ~Monitor the efficiency of the pharmaceutical quality system (PQS), establish relevant KPIs to monitor the efficiency, define and implement... 

 ...Managing changes and deviations, as well as corrective and preventive actions in consultation with QA. ~Provide expert support to monitor, update, and adapt the GMP-relevant document landscape within pCMC. ~Participating in the preparation and coordination of internal... 

 ...Instruction for Use (IFU) documentation. ~Familiarity with process development and regulatory considerations in parenteral Drug Product clinical-grade manufacturing is considered a significant asset. Would you like to learn more about CTC and the opportunity outlined?... 

 ...centralized L&D function. ~Facilitate communication and training programs to ensure smooth adoption of new L&D processes and tools. ~Monitor and report on the progress of the implementation, adjusting strategies as necessary to address challenges. 6. Continuous... 

 ...escalation •Ensures tracking of business deliverables and accountable for business readiness and business data quality •Tracks and monitors continuity of Data Cleansing activities together with the business teams with corresponding reporting •Guides the involved Team... 

 ...analysis of reported incidents •Communicating and coordination of End User activities if there is a major incident •Interface Monitoring (Business Errors) •Support Execution of system actions •Support Implementation of new Systems and Equipment •Continuous Improvement... 

 ...team of the client. You will be required to support and lead the drug product development of various oral products entering their clinical pipeline more especially for late-stage development and commercial oral dosage forms.   Main Responsibilities: ~Lead the technical... 

 ...EASA DOA surveillance audits and annual meetings, including preparation, coordination, participation, tracking of findings/CARs and monitoring implementation of corrective actionsSupport the management of suppliers that perform design activities as well as support of the... 

 ...trademark registrations procedures and regulations before IGE and WIPO Familiar with the most commonly used trademark search and monitoring tools Excellent communication and writing skills Fluent in English and German, French is an advantage Please note that... 

 ...all applicable trade compliance regulations in order to guarantee on time deliveries from and to PilatusObtaining, managing and monitoring export licenses throughout the supply chains in compliance with regulations, including issuing, obtaining and administrating required...