BrightOwl Loader Loading

Clinical Research Associate Warsaw Poland,  

KCR (company)


Posted on : 08 March 2017

Project Description


 
The duties associated with the role include:
  • Performing site visits and monitoring activities in accordance with protocol, GCP/ICH Guidelines and other applicable requirements 
  • Ensuring overall integrity of study and adherence to guidelines, protocol and regulations 
  • Taking an active role in the project team by providing feedback and suggestions for successful completion of the project 
  • Coaching and mentoring less experienced CRAs to assist in their development and training  


Requirements:
  • University degree in life sciences/pharmacy/biotechnology 
  • At least 1 year of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines 
  • Computer competency 
  • Fluent command of English 
  • Ability to complete tasks in an accurate and timely manner  

Locations

Poland Warsaw

Find a Job Find Candidates

Similar Jobs

More jobs from KCR

Other jobs in Poland

Other jobs in Warsaw

Other jobs from KCR in Warsaw

Other similar job in Warsaw

Other Jobs

Most Recent Searches

Most Famous Searches

You might also like