Site Monitoring Specialist

Job Overview">We are looking for a skilled Research Associate - Site Management Specialist to join our team. In this role, you will be responsible for managing and monitoring clinical trials across various sites.">Key Responsibilities:">Conduct site monitoring visits to ensure compliance with study protocols and regulations.Develop and implement subject...

Work Location: Various locations across NorwayCandidates preferable location: Norway or Poland (possible relocation from Poland to Norway)Contract Type: Full-time, long-term, work in rotationsABOUT USWe are Forces DC – a leading provider of skilled workforce delivering structured teams of specialists for the data center construction projects in Nordics and...

Role Overview:This is an exciting opportunity to join our Clinical Operations team in Norway as a Clinical Research Associate. In this role, you will be responsible for monitoring and managing clinical trials, working closely with Investigators, patients, and other stakeholders to ensure the success of our studies.Key Responsibilities:Conduct site visits and...

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About TN NorwayJob DescriptionWe are looking for a Clinical Research Associate to join our team at TN Norway. In this role, you will be responsible for overseeing the conduct of clinical trials at study sites.Main ResponsibilitiesPerform site monitoring visits to ensure compliance with GCP and ICH guidelines.Collaborate with sites to develop and track...

Work Location: Various locations across NorwayCandidates preferable location: Norway or Poland (possible relocation from Poland to Norway)We are looking for an experienced Site Manager to lead teams on ongoing projects across various locations in Norway.**Your Role**Coordinate daily work of teams consisting of electricians, fitters, and other technical...

Job DescriptionThis challenging role involves monitoring Nodnett transmission, base station, control room and core network elements using developed tools. As a system administrator, you will be responsible for identifying and interpreting alarms, prioritizing them, and taking appropriate action.You will need to provide first-line investigation support on...

About Our TeamWe are a dynamic team at IQVIA Argentina, working together to deliver high-quality clinical research services to our clients. As a Research Site Management Expert, you will play a key role in ensuring the successful management of our research sites.The ideal candidate will have a strong understanding of GCP and ICH guidelines and at least 2...

Social network you want to login/join with:At Alstom, we understand transport networks and what moves people. From high-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the industry. Every day, more than 80,000 colleagues lead...

**Key Responsibilities:**The ideal candidate will have at least 3-4 years of independent clinical trial monitoring experience, a high level of knowledge of ICH GCP Guidelines, and fluent local language and English, both written and spoken.Requirements:University degree, preferably in medical or life sciences; nursing education or other relevant healthcare...