Clinical Research Coordinator
| Company | Ohio State University – Columbus |
|---|---|
| Location | Columbus, OH, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Junior |
Requirements
- Bachelor’s Degree in biological sciences, health sciences or related field required or equivalent combination of education and experience required
- One year experience in a clinical research capacity conducting clinical research studies required
- Computer literacy with basic database tools and methods required
Responsibilities
- Assists in the coordination and oversight of trials in the acute leukemia and other hematologic malignancy patient population
- Identifies and assesses eligibility of patients for clinical research study participation
- Obtains informed consent via both in person and remotely
- Educates patients and their family members on the diagnosis and discusses clinical research studies
- Monitors study participants and ensures proper follow-up visits are scheduled and conducted
- Oversees and prepares for external quality assurance and control review
- Collaborates with sponsoring agencies
- Collaborates and serves as liaison with an inter-disciplinary research team
- Designs database components and reporting tools
- Completes data entry and monitors data quality with assurance and quality control
- Develops detailed reports for data related to strategic decision-making, research, publications, or presentations; analyzes, queries, interprets and summarizes data for principal investigators (PI)
- Prepares proposals requesting further clinical research
- Executes and oversees technical processes to collect and extract data
- Makes recommendations to PI based upon data analysis
- Maintains patient inventory in Oncore, assists the PI in writing manuscripts and in preparation of grant submission
- Creates and maintains tools and work flows for research with clinic and faculty
- Educates the hospital staff and non-Hematology physicians on the study protocols and purpose of the study
- Works with the PI in developing plans to meet the requirements of new clinical research studies issued by different laboratories and to meet research requests from various physicians
- Responsible for review of institutional review board(IRB) submissions
- Participates in ensuring protocol compliance with all federal, local and institutional regulations
- Assists with research sample collection including blood draws
Preferred Qualifications
- Prior clinical research database management desired