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Job Details

Covance Romania is looking for Clinical Research Associates! (all levels for our Bucharest office)

Company: Covance
Reference: 63724BR
Closing Date: 05 Nov 16
Type: Permanent
Salary (£): Competitive

Job Summary:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.


You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance's impressive history of company stability and growth. We've achieved these results by fostering a work environment that encourages, develops and leverages our team's capabilities. 

This is your chance to become part of a team that helps to bring miracle of medicine to market sooner. 

At the moment we are looking for Clinical Research Associates of all levels for our Bucharest office. 

As CRA you will be responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits. 


  • Site administrating and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP;
  • Recruiting potential investigators, preparing EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor; 
  • Completing Serious Adverse Event (SAE) reporting, processing production of reports; 
  • Negotiating study budgets with potential investigators and assisting the Covance legal department with statements of agreements as assigned; 
  • Interact with internal work groups to evaluate needs, resources and timelines; 
  • Assist with training, mentoring, and development of junior employees, e.g. co-monitoring; 
  • Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned. 

Education/Qualifications Required: 

  • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology 
  • Few years of relevant clinical research experience in pharmaceutical or CRO industries will be considered (including pre-study, initiation, routine monitoring and closeout visits) 
  • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries 
  • Experience within oncology therapeutic area (preferable) 
  • Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs 
  • Excellent site monitoring skills 
  • Excellent study site management skills 
  • Excellent registry administration skills 
  • Ability to work with minimal supervision 
  • Good planning and organization skills 
  • Good computer skills with good working knowledge of a range of computer packages 
  • Excellent verbal and written communication skills 
  • Ability to resolve project-related problems and prioritizes workload for self and team 
  • Fluent Romanian and English language skills 


Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to

Apply for this job: Covance Romania is looking for Clinical Research Associates! (all levels for our Bucharest office)

Contact Information:

Address:  Covance- Warsaw

Website:  Visit Our Web Site

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