Clinical Research Coordinator-Hematology

The Ohio State University • Columbus, OH

1d

About The Position

Clinical Research Coordinator responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies, within the Division of Hematology; coordinates clinical research activities to include identifying and assessing eligibility of patients for clinical research study participation; discussing research studies with patients and their family members; obtains informed consent and assists with IRB submissions, modifications and amendments; collaborates with an interdisciplinary research team made up of members from the Division of Hematology, other personnel within the OSUWMC, as well as external; ensures that all necessary data is collected and reported as appropriate; provides support to the members of the clinical research team in developing plans to meet the requirements of new clinical research studies; participates in writing manuscripts and in preparation of grant submissions; researches, develops and creates detailed reports and presentations in response to data and reporting requests; participates in internal and external quality reviews; analyzes, queries, interprets and summarizes data; collects and extracts data; ensures and verifies data integrity. Generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors.

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

• Identifying and assessing eligibility of patients for clinical research study participation
• Discussing research studies with patients and their family members
• Obtains informed consent and assists with IRB submissions, modifications and amendments
• Collaborates with an interdisciplinary research team
• Ensures that all necessary data is collected and reported as appropriate
• Provides support to the members of the clinical research team in developing plans to meet the requirements of new clinical research studies
• Participates in writing manuscripts and in preparation of grant submissions
• Researches, develops and creates detailed reports and presentations in response to data and reporting requests
• Participates in internal and external quality reviews
• Analyzes, queries, interprets and summarizes data
• Collects and extracts data
• Ensures and verifies data integrity
• Generates reports and reviews to ensure validity of data
• Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations
• Assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors

Benefits

• Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
• Paid time off, including sick and vacation time and 11 holidays.
• State retirement plan or an alternative retirement plan, both with generous employer contributions.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees