Hordaland

i-Pharm Consulting Ltd

Clinical Research Associate/CRA required for well-established international CRO based in Norway. We are looking for a candidate for a full time position to be either office-based or home-based. You will be monitoring sites across Norway. It is an excellent opportunity to join global CRO with a life-work balanced position. The role can be at CRA (Clinical Research Associate) II or Senior CRA (Clinical Research Associate) level.

You will implement and monitor clinical trials in Norway. Conduct all types of visits from pre-study to close-out. Perform source document verification and case report form review. Conduct study drug inventory. Assess patient recruitment and retention.

JAPP

Er du interessert i helse og skjønnhet? Liker du å gi helse- og skjønnhetstips til andre?

Nå lanserer vi et nytt velværekonsept som vektlegger helse både på inn- og utsiden, og vi søker derfor selgere i hele Norge. Du kommer til å jobbe med forskjellige helse- og hudpleieprodukter av høyeste kvalitet som på en enkelt måte gir bedre helse og velvære til brukerne av produktene du selger.

Arbeidet er fritt og inspirerende, og du bestemmer selv arbeidstiden og mengden. Arbeidsinnsatsen din blir godt belønnet. Du bestemmer selv om pengene du tjener skal anses som ekstra- deltid-, eller fulltidsinntekt.

ConnectWith, Oslo, Bergen or Ålesund

One of the worlds leading Facilities Management service providers is urgently seeking a Facilities Co-ordinator to join their rapidly growing business ion Oslo. You must have a solid track record in Facilities Management and speak fluent Norwegian and English. You will be responsible for creating all work orders across 48 sites in Norway. This will include maintenance of the clients facilities. You will need to organise labour to fulfil each work order by using both internal and external resources. This will include getting quotes and selecting the correct supplier.

Tasks

• Operations management
• Administrative responsibility
• Internal & external reporting
• Work order system management

inVentiv Health Clinical recruiting on behalf of client

As a Clinical Research Associate you will be at the forefront of the clinical trials practice. As a member of our Clinical Research Team you will reflect its unique characteristics and help world class companies to ensure the right size and custom fit for their trial needs. This is an excellent opportunity enabling you to take your careers and skills to the next level working for the world's largest healthcare clients.

Responsibilities:

• Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 - 50% travel) for GCP compliance according to inVentiv Health SOPs and/or client guidelines
• Recruit investigators for participation in clinical trials
• Negotiate study budgets with investigators

Concertare Beratungs- und Dienstleistungsgesellsch

We are looking for mystery shoppers all over Sweden/Norway to conduct mystery calls and test the service quality of major car brands.

We are a market research company located in Germany specializing in Mystery Shopping. Requirements:

• Excellent observation skills
• Dependability
• Language Skills: English

inVentiv Health Clinical recruiting on behalf of client

As a Clinical Research Associate you will be at the forefront of the clinical trials practice. As a member of our Clinical Research Team you will reflect its unique characteristics and help world class companies to ensure the right size and custom fit for their trial needs. This is an excellent opportunity enabling you to take your careers and skills to the next level working for the world's largest healthcare clients.

Responsibilities:

• Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 - 50% travel) for GCP compliance according to inVentiv Health SOPs and/or client guidelines
• Recruit investigators for participation in clinical trials
• Negotiate study budgets with investigators
• Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites