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Clinical Research Monitor

Régió: Budapest

HAYS Hungary Kft.
Hozzáadva: 2017.12.01.
Jelentkezési határidő: 2017.12.12.
Hirdetés azonosító: 1177500

 

 
 
Clinical Research Monitor
Our partner is looking for a clinical research monitor to join to their team. The main aim of the position is to   oversight of clinical research conducted at sites to ensure compliance with study protocols, applicable regulatory standards.

The main responsibilities of the clinical research monitor are:

  • Performing site monitoring visits in accordance with the study Monitoring Plan to ensure compliance with the investigational Plan.
  • Preparing site visit reports and correspondence for all visits conducted in accordance with the study Monitoring Plan.
  • Communicating visit findings with site personnel, ensure relevant follow-up.
  • Identification and escalation of protocol deviations, discrepancies in data, and non-compliance to study protocols, applicable regulations, Good Clinical Practices and Standard Operating Procedures.
  • Identifying site needs, providing solutions to facilitate the clinical trial process.
  • Acting as a primary point of contact for study sites as requested.
  • Assisting in initial and ongoing site personnel training as required.
  • Possessing a working knowledge of disease state and investigational product.
  • Attending Investigator and/or Coordinator meetings.
  • Leading all relevant monitor responsibilities.

The main requirements of the clinical research monitor will be:

  • Bachelor’s Degree in life sciences, nursing or other health related disciplines.
  • Min. 2 years of Clinical Research experience.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
 

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