Clinical Research Coordinator-Hematology
About The Position
The Clinical Research Coordinator is responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies, primarily in observational studies, within the Division of Hematology. This role involves coordinating clinical research activities such as identifying and assessing patient eligibility for study participation, discussing research studies with patients and their families, obtaining informed consent, assisting with data quality control, scheduling and conducting monitoring visits, and query resolution. The coordinator will also be involved in participant screening, recruitment, and bio-specimen collection. Additionally, they will assist with IRB submissions, modifications, and amendments, and collaborate with an interdisciplinary research team from the Division of Hematology, other OSUWMC personnel, and external entities. The role ensures all necessary data is collected and reported appropriately, supports the research team in developing plans for new studies, and participates in writing manuscripts and preparing grant submissions. Responsibilities include researching, developing, and creating detailed reports and presentations, participating in internal and external quality reviews, analyzing, querying, interpreting, and summarizing data, and ensuring data integrity. The coordinator will generate reports and reviews to ensure data validity and support activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state, and industry sponsor regulations. They will also assist with coordinating and preparing for external quality assurance and control reviews.
Requirements
- Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required.
- 1 year of relevant clinical research experience required.
Nice To Haves
- 2-4 years of relevant experience preferred.
Responsibilities
- Coordinate and oversee clinical research protocols investigating hematology malignancies.
- Identify and assess eligibility of patients for clinical research study participation.
- Discuss research studies with patients and their family members.
- Obtain informed consent.
- Assist with data quality control, scheduling and conducting monitoring visits, and query resolution.
- Screen, recruit, and collect bio-specimens from participants.
- Assist with IRB submissions, modifications, and amendments.
- Collaborate with an interdisciplinary research team.
- Ensure all necessary data is collected and reported as appropriate.
- Provide support to the clinical research team in developing plans for new clinical research studies.
- Participate in writing manuscripts and in preparation of grant submissions.
- Research, develop, and create detailed reports and presentations.
- Participate in internal and external quality reviews.
- Analyze, query, interpret, and summarize data.
- Collect and extract data.
- Ensure and verify data integrity.
- Generate reports and reviews to ensure validity of data.
- Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state, and industry sponsor regulations.
- Assist with coordinating and preparing for external quality assurance and control reviews.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
