Clinical Research Associate, Czech Republic - 133768

This is a great chance to join a global leader and will suit someone, who wants to work for the best, receive good training and be part of an experienced team.

This opportunity is suitable for CRAs who have previous clinical trials/ monitoring experience.

As a Clinical Research Associate your main duties will be:
• Perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH, GCP, FDA Guidelines, local regulations and PPD SOPs
• Conduct site visits to assess protocol and regulatory compliance and manage required documentation
• Represent PPD and develop and maintain collaborative relationships with investigational sites
In order to be successful for this role you need:
• Bachelor's degree in a science related field
• Proven clinical monitoring experience
• Good organizational and time management skills
• Effective interpersonal skills
• Good English language skills- both verbal and written

HOW TO APPLY:

Please submit your CV in English.

Registration on our website will also give you the opportunity to be considered for other positions if this one is not the most appropriate for your qualifications and experience.

This is an ongoing search. Suitable candidates will be contacted accordingly.