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CRAs in Europe - Switzerland, Germany, Italy, United States  

Meditrial Europe (company)


Posted on : 05 May 2017

Project Description

description:
  • our company  offers great opportunities for Clinical Research associates (Research_Associate" rel="nofollow">CRAs), in full time or Freelancer" rel="nofollow">Freelance positions in europe. 
  • we offer attractive income potential, outstanding Career progression and exposure to cutting-edge Training and technology.    


profile    
the basic experience which we require are:     


positions   
  • Research_Associate" rel="nofollow">CRA i minimum of 2 years experience as crc or cta or equivalent 
  • Research_Associate" rel="nofollow">CRA ii (senior) 3-5 years experience) 
  • Research_Associate" rel="nofollow">CRA iii (Expert)  >5 years    


benefits    
our Research_Associate" rel="nofollow">CRAs enjoy:     
  • a Clinical team approach to supporting sites, resulting in our Research_Associate" rel="nofollow">CRAs being responsible for less administrative and site management tasks 
  • access to dedicated Training courses and cutting-edge continual Education programs 
  • Career advancement as a Research_Associate" rel="nofollow">CRA and home-based management opportunities 
  • advantages of working as a Research_Associate" rel="nofollow">CRA with the company
  • Flexibility to work in a remote-based capacity for most Research_Associate" rel="nofollow">CRA positions 
  • virtual initial and ongoing Training via our latest-generation webex platform and CTMS system 
  • smartphone provided by the company (or the ability to use your own iphone or android smartphone for business use with a monthly Reimbursement
  • frequent flyer miles retained by the Employee for personal use.   
  • a nights out  reward program for frequent travelers (travel 25 to 30 nights per quarter) you choose between e.250 or one additional day of paid time off    


job description  
  Research_Associate" rel="nofollow">CRAs play a vital role in meeting our commitment to our clients. they are responsible for:     
  • conducting site initiation and Investigator Training 
  • reviewing study case report forms (crfs) completed by the investigative sites, and verifying entries by validating accurate source Documentation to support crf entries 
  • documenting site visits and issues in reports and follow-up letters to the site 
  • facilitating effective Communications among investigative sites, the client and the company.
  • identifying potential Investigators in collaboration with the client 
  • responding to company, client and national regulatory requirements/audits 
  • contributing to the project team by assisting in project Communications, in close collaboration with the Clinical team members    



compensation    
  • for Employees, a competitive base salary and bonus program are available. 
  • for Freelancer" rel="nofollow">Freelance positions, fees based on %fte, daily rates and collaboration opportunity.   
  • compensation is commensurate with experience and will be discussed with qualified candidates only.    



who we are    

Locations

Hünenberg Switzerland Berlin Germany Rome Italy New York USA

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