Clinical Research Coordinator I, Radiation Oncology, GU-Prostate Cohort
About The Position
This position works within the Clinical Research Program of the Department of Radiation Oncology and supports the research team in the overall conduct of clinical trials. We are seeking an energetic, organized, and detail-oriented individual to support a portfolio of multidisciplinary clinical research projects. The program leadership is committed to training and inspiring the next generation of healthcare leaders and clinicians, working on important clinical and healthcare issues—ranging from making the delivery of care safer and more efficient, to expanding health insurance coverage and eliminating disparities, to improving the performance of entire health systems. Provides assistance to the Principal Investigator and Study Team in coordinating research activities that may include conducting a variety of clinical research projects with established methodologies, data collection and management, and other research activities as assigned. Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. This position is ideal for candidates planning to pursue medical or other graduate-level training. Applicants must be able to commit to a minimum of two years in the role.
Requirements
- Bachelor's Degree Related Field of Study required
- Some relevant research project work 0-1 year preferred
- Careful attention to detail and good organizational skills.
- Ability to follow directions.
- Good interpersonal and communication skills.
- Computer literacy.
- Working knowledge of clinical research protocols.
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Responsibilities
- Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
- Recruiting patients for clinical trials and conducting phone interviews.
- Verifies the accuracy of study forms and updates them per protocol.
- Prepares data for analysis and data entry.
- Documents patient visits and procedures.
- Assists with regulatory binders and QA/QC Procedures.
- Assists with interviewing study subjects.
- Assists with study regulator submissions.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
