Clinical Trials Research Associate
3 weeks ago
The University of Iowa Hospitals & Clinics is seeking a highly skilled Clinical Trials Research Associate to join our team at the Holden Comprehensive Cancer Center. As a key member of our Clinical Trials Research team, you will play a crucial role in coordinating clinical oncology study activities, including planning, delivery, and evaluation of healthcare provided to research protocol patients.
Key responsibilities will include assisting Clinical Research Coordinators in data collection, collaborating with multiple departments and offices, maintaining medical documentation, and managing data entry and electronic data systems for clinical research protocols and laboratory investigations.
You will also serve as a member of the Clinical Research Services team, planning, delivering, and evaluating healthcare provided to research protocol patients. Additionally, you will create, populate, maintain, and enhance multiple databases containing clinical and research information, ensuring compliance with Institutional Review Board requirements and physician needs.
Other key responsibilities will include assisting in the design, development, execution, and administration of data gathering and data entry for clinical trials, as well as educating study participants on the scope of study and schedule of assessments.
You will also be responsible for entering subject data on electronic databases, ensuring all prerequisites have been completed and are within required parameters. Furthermore, you will manage the collection of data, including maintaining records of patient visits/interviews, documentation of adverse events, and review of medication records.
**Key Requirements:**
- Bachelor's degree or equivalent combination of education and experience
- Minimum 1 year experience in a research setting
- Experience with medical terminology
- Proficient in computer software applications
- Ability to organize and evaluate complex medical information and data
- Experience with adult oncology patients
- Experience coordinating clinical research studies
- Knowledge of regulatory guidelines and procedures
- Clinical Research Coordinator Certification (SOCRA or ACRP)
- Experience working with Epic and OnCore Clinical Trials Management System
**What We Offer:**
- Competitive salary and benefits package
- Opportunities for professional growth and development
- Collaborative and dynamic work environment
**How to Apply:**
To be considered for this exciting opportunity, please upload your resume and cover letter, clearly addressing how you meet the required and desired qualifications of this position.
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