Country: Hungary
Functional area: Clinical Research
Clinical Research Associate is urgently needed at our mid-sized CRO partner. The role will have end-to-end responsibility for clinical studies from feasibility to close-out.
Besides clinical drug development in various therapeutic areas you will have the opportunity to participate in nutritional and medical device related trials as well.
This is a home-based or semi home-based role and ideal candidates are based in Budapest or Pest county.

Responsibilities:
  • Full-cycle responsibility for clinical studies
  • Participates in feasibility and study startup activities.
  • Gets involved in regulatory phase (Clinical Trial Application)
  • Drives site management activities (site selection, initiation, monitoring and close-out)

Requirements:
  • University degree in Life Sciences discipline
  • Proven track record in clinical research including at least 1 year independent monitoring experience
  • Knowledge of ICH GCP and regulatory guidelines
  • Ability to develop and maintain effective working relationship with investigators and other stakeholders
  • Strong attention to detail, good organizational skills and ability to meet deadlines
  • Fluent English and Hungarian

Should you be interested in the details of this vacancy please submit your CV.
Clinical Research Associate is urgently needed at our mid-sized CRO partner. The role will have end-to-end responsibility for clinical studies from feasibility to close-out.
Besides clinical drug development in various therapeutic areas you will have the opportunity to participate in nutritional and medical device related trials as well.
This is a home-based or semi home-based role and ideal candidates are based in Budapest or Pest county.

Responsibilities:

  • Full-cycle responsibility for clinical studies
  • Participates in feasibility and study startup activities.
  • Gets involved in regulatory phase (Clinical Trial Application)
  • Drives site management activities (site selection, initiation, monitoring and close-out)

Requirements:

  • University degree in Life Sciences discipline
  • Proven track record in clinical research including at least 1 year independent monitoring experience
  • Knowledge of ICH GCP and regulatory guidelines
  • Ability to develop and maintain effective working relationship with investigators and other stakeholders
  • Strong attention to detail, good organizational skills and ability to meet deadlines
  • Fluent English and Hungarian

Should you be interested in the details of this vacancy please submit your CV.on-site monitoring ICH GCP clinical research