Clinical Research Associate

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 Poland.

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 Polish 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
To apply for this position email us your CV along with a cover letter to cv@dokumeds.com.