Clinical Trial Assistant

If you are a growth-oriented biomedical professional with strong organizational skills and an excellent command of English, we would like to hear from you.


  • Supports the clinical research teams with ongoing conduct of clinical trials
  • Assists project teams with study-specific documentation as appropriate
  • Assists in the preparation, handling and tracking of Ethics/Regulatory submissions
  • Maintains the study files for the project
  • Coordinates ordering/dispatch of clinical trial materials to domestic and/or international sites
  • Conducts needs analysis and recommends corrective action for training and development
  • Reviews regulatory documents while ensuring compliance with Good Clinical Practice (GCP) rules and regulations
  • Contacts sites to resolve study-related issues and to monitor progress in completing regulatory documents
  • Prioritizes study-related tasks for multiple projects to meet project deadlines and other deliverables


  • A Bachelor degree in life sciences or IT is preferred
  • Fluency in English is mandatory
  • Excellent organizational and administration skills
  • Excellent verbal and written communication skills
  • Computer literacy, proficiency in MS Office, knowledge with imaging software is an advantage


  • Competitive remuneration package
  • Training and growth opportunities, international exposure

Job Status: Full time

Contact person: Dr. Dimitar Mirchev

Please, send your resume, a cover letter and a copy of your diploma to or alternatively mail them to:

Dr. Dimitar Mirchev
6 Tri Ushi Str., Office 2
1000 Sofia, Bulgaria

Confidentiality of applications is guaranteed.