Dokumeds is looking for highly motivated and proactive full time employee willing to develop together with the company in position of Clinical Research Associate in Ukraine.
Main responsibilities:
- Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor Standard Operating Procedures, legal requirements and ICH-GCP Guidelines
- Conduct of country and site feasibility
- Site initiation, routine monitoring and close-out visits
- Support in preparation and submissions to Ethics Committees/ Regulatory Authorities
- Assistance in site contract management
Requirements:
- University degree in medicine, pharmacy, nursing or life science
- Minimum 2 years of previous on-site monitoring experience in CRO or Pharma company
- Thorough knowledge of ICH-GCP guidelines including an understanding of local regulatory requirements
- Previous experience in preparation and submissions to Ethics Committees/ Regulatory Authorities will be considered as advantage
- Excellent knowledge of English and Ukrainian languages
- Availability to travel
- Computer literacy
- Driving license
- Strong organizational, communication and teamwork skills
We offer:
- A job with daily exciting challenges in a highly qualified and international team
- Employee-friendly work environment
- Competitive salary
- Opportunity to learn and grow professionally in Clinical Research field