Clinical Research Associate (CRA)

Location
Sweden
Salary
competitive salary + benefits
Posted
11 Jun 2021
Closes
30 Jun 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Entry level

Responsibilities

  • Responsible for the set-up, monitoring, and close-out of clinical trial sites in Sweden
  • Trial start up activities; ethics submissions, site feasibility, site contract negotiations, supporting vendor selection, and development of study tools.
  • Monitoring includes site selection/qualification, routine monitoring, and site close-out visits conducted per the Monitoring Plan.
  • Produce accurate and complete monitoring reports
  • Verifying compliance with the Clinical Trial Protocol, GCP, and other relevant requirements at the sites.

Qualifications

  • Life sciences Degree
  • Min 1 year experience working as a CRA, monitoring across all types of visits - feasibility, initiation, monitoring and close out.
  • Oncology experience preferred
  • Client facing, and customer service experience