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.
Responsibilities:
- 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
Qualifications:
- 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
Benefits:
- 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 careers@convex.bg or alternatively mail them to:
Dr. Dimitar Mirchev
6 Tri Ushi Str., Office 2
1000 Sofia, Bulgaria
Confidentiality of applications is guaranteed.