Clinical Research Coordinator

# Clinical Research Coordinator Children's National Hospital Full Timemid Montgomery, Alabama, USPosted Yesterday##

Role Overview Children's National Hospital is hiring a mid-level Clinical Research Coordinator. This is a full-time role in Montgomery. posted yesterday. Full responsibilities, required qualifications, and the apply link are listed in the description below.## Resume Keywords to Include Make sure these keywords appear in your resume to improve ATS scoringGCPORInventory Compensation Benefits Compliance Kids Everything Sign  up free to auto-tailor your resume with all these keywords and get a higher ATS score##

Job Description Kids Are Our Everything.

Department
10266 Neuroscience Research Admin Pay Range $51,584.00 - $85,987.20

The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Research Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.

This position may direct the work of junior staff, train personnel and direct the work of a Clinical Research Assistant as assigned.

Minimum Education B.A./B.S. degree in a science, technical, health-related field or other applicable discipline (Required)
Minimum Work Experience1 year of applicable work, research or internship experience (e.g. research assistant, data manager, clinician or other interaction with a research population). (Required)
Functional Accountabilities Responsible Conduct of Research
* Consistently demonstrates adherence to the standards for the responsible conduct of research.
* Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
* Stays informed of and adheres to institutional policies and federal regulations (e.g. Titles 21 and 45 of the Code of Federal Regulations) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information.
* Uses research funds and resources appropriately.
* Maintains confidentiality of data as required.
* Meets all annual job-related training and compliance requirements.

Research Administration
* Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.
* Accurately creates, completes, maintains and organizes study documents.
* Accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.
* Uses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.
* Reviews current literature to obtain information relevant to clinical research program, as directed.
* Attends study meetings, which could include overnight travel, as requested by principal investigator.
* Works well with other members of the research team and seeks and provides input when appropriate.
* Serves as an effective liaison between the investigators, sponsors, hospital departments involved with research studies and the Clinical Research Center.

Participant Enrollment
* Employs strategies to recruit and retain research participants, while adhering to the IRB-approved recruitment plan.
* Screens subjects for eligibility per the protocol and institutional policies.
* Communicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.
* Independently coordinates, conducts and documents visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments and SOPs for minimal risk studies or for other studies under direction.
* Interacts with study participants and/or legally authorized representatives (LARs) to communicate study…