Clinical Research Associate (CRA)
The Clinical Research Associate (CRA) from IMARC Research, Inc. will work with a Sponsoring company or CRO in the monitoring of medical device, biologic, and pharmaceutical trials with an emphasis placed on ensuring the highest ethical and clinical standards.
Must be willing to relocate to Cleveland, OH or Minneapolis, MN area.
The Clinical Research Associate will monitor clinical research sites in accordance with FDA Regulations, Good Clinical Practice, company SOPs, and client guidelines.
Clinical Research Associate
Monitoring responsibilities: The primary focus of this position is on routine monitoring and management of the research-related activities at a clinical site. Once fully trained, a Clinical Research Associate will be expected to perform site initiation, periodic, and close-out visits. Additionally, the Clinical Research Associate will be expected to serve as a resource and research liaison between assigned sites and the Sponsoring companies or CROs.
Knowledge, Skills, and Abilities:
The following knowledge and skills are preferred:
Salary commensurate with experience.
Job Type: Full-time