A company is looking for an In-House Clinical Research Associate in Poland.
Key Responsibilities
Support site management activities and ensure compliance with protocol requirements
Conduct remote data reviews and assist with data query resolution
Coordinate study visits and manage clinical trial supplies for investigative sites
Required Qualifications
Undergraduate university degree (Bachelor or Honors Bachelor)
1-3 years of related experience in clinical research
Initial and ongoing training in clinical research practices
Familiarity with ICH GCP and regulatory standards
Experience with site management and monitoring activities
Clinical Research Associate • Saint Paul, Minnesota, United States