Title: Clinical Research Associate (CRA) - A
Location: Lake Forest, Illinois
Duration: 12+ Month Assignment
Position will be remote (first several weeks will be onsite)
Responsibilities:
- Support clinical study activities including study data monitoring, updating/maintaining study documentation.
- Member of the clinical team responsible for conducting single or multi center studies according to Federal Regulations and ICH guidelines.
- Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) management, training of investigator sites, planning and running study meetings, evaluation, training of new study investigators.
- Responsible for writing basic study protocols, monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary.
Qualifications:
- Bachelor’s degree / 1-3 years Top 5 skills/requirements
- Clinical Trial Management, Data Management systems, Informed Consent, GCP, Case Report Forms, Verbal & Written Skills.
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.