Clinical Research Support Associate

23 hours ago


Solna Municipality, Sweden TN Sweden Full time

Key Responsibilities and Qualifications

  • Assist CRAs and RSU teams with clinical document management and system maintenance.
  • Prepare and distribute clinical documentation and reports.
  • Track and manage CRFs, queries, and clinical data flow.
  • Act as a central contact for the clinical team.
  • Participate in site visits.

Required Skills and Experience

  • High School Diploma or equivalent.
  • Administrative support experience.
  • Microsoft Office proficiency.
  • Excellent written and verbal communication skills.
  • Time management and organizational skills.
  • Knowledge of clinical research regulatory requirements.


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