EastHORN Clinical Services in CEE Ltd is a clinical contract research organisation (CRO) serving global pharmaceutical and biotechnology companies in the development of new medicines. The company has operations throughout Central and Eastern Europe.

Our international clients value our enthusiastic and flexible approach to meeting their needs and we are growing rapidly. To support our further growth we are looking for a

Clinical Research Associate

Responsibilities include but are not limited to:

• identification of investigators and site selection; conducting pre-study visits for qualification of investigators and sites; compiling regulatory packages

• conducting all types of monitoring, including but not limited to, routine monitoring, close-out and audit visit attendance; verifying clinical data against source documentation during routine monitoring

• completing monitoring trip reports, reports study progress, escalating issues related to the protocol according to EastHORN and/or Sponsor timelines and quality

• conducting on-site investigational product and study supply accountability and management

• facilitating communication between Investigator and Sponsor

• preparing and negotiating study budgets for the site, investigator, and study vendors

• preparing, organizing, and overseeing site, investigator, and vendor payments

Requirements:

• 1-2 years’ experience in clinical trials area will be considered an advantage

• Master Degree in life sciences (medicine, pharmacy, biology, chemistry or related)

• Excellent level of written and spoken English

 

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