This role is open to current Clinical Research Associates with 3 + years
experience and based in Turkey only.
As a top Clinical Research Organization in the world, we are looking to strengthen our Clinical Operations team. You will work independently and actively manage all necessary activities required for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation.
Dedicated to one sponsor, a global pharmaceutical company that leads the way in discovering and developing innovative health solutions that help prevent and treat diseases in animals and people.
Our sponsor has a long history of excellence in research, delivering medicines, vaccines, and other health solutions for some of the most difficult diseases in the world.
You Will Possess:

• Bachelor's degree in a life science or related discipline.
  
• At least 1 year of monitoring in the advertised country.
  
• Essential - minimum of 3 years of active independent field monitoring experience as a CRA - all types of visits.
  
• Deep understanding of ICH GCP Compliance.
  
• Excellent time management and social skills
  
• Initiative-taking with a phenomenal eye for detail.
  
• Ability to travel.
  

Benefits Of Working with Parexel FSP

• Comprehensive benefits package including premium salary.
  
• Car option
  
• Company cell phone and equipment.
  
• Market leading PTO.
  
• Culture of teamwork and collaboration.
  
• Local line manager.
  
• Excellent training.
  
• People who motivate and face challenges together.
  
• Innovative technology.
  

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set.
Apply today.
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