Iterative Scopes, Inc
RN Research Coordinator Flowood, MS
Iterative Scopes, Inc, Jackson, Mississippi, United States
Overview
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network includes 70+ clinical research sites across the US and Europe focused on GI and hepatology therapies. We empower partner sites with tech-enabled services to drive success and growth by combining clinical trials expertise with AI to accelerate access to novel therapeutics for patients in need. Position purpose
The Nurse Research Coordinator is a specialized research professional working with and under the direction of the Director and Clinical Principal Investigator (PI). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. Responsibilities
Communicate study requirements to all individuals involved in the study. Develop and implement recruitment strategies in accordance with Impact Research and IRB requirements and approvals. Screen subjects for eligibility using protocol specific inclusion and exclusion criteria. Enter participant information and study visit procedures into the Clinical Trial Management System to ensure billing to the appropriate funding source. Maintain adequate inventory of study supplies; when handling investigational drugs/devices, follow sponsor protocol and Impact Research policy on accountability. Complete study documentation and maintain study files per sponsor requirements and Impact Research policies, including consent forms, source documentation, case report forms, and accountability forms. Maintain effective communication with sponsor, research participants, Director and PI during the course of the study. Manage daily study activities, problem-solve, and manage protocol coordination. Collect and report ongoing patient recruitment/enrollment metrics to Director and PI. Arrange secure storage of study documents in accordance with Good Clinical Practice guidelines or as required for the contracted length of time. Protect the rights and welfare of all human research participants in accordance with Federal regulations. Cooperate with compliance and monitoring efforts regarding PHI access, use, and disclosure and report noncompliance as required. Other duties as assigned. Qualifications
Experience:
RN license required; 1-3 years of Clinical Research Coordinating experience preferred. Other Requirements:
None Performance requirements
Knowledge of grammar, spelling, and punctuation. Knowledge of purchasing, budgeting, and inventory control. Skill in taking and transcribing dictation and operating office equipment. Skill in answering the phone and responding to questions. Skill in time management, prioritization, and multitasking. Skill in writing and communicating effectively. Ability to work under pressure and present information clearly. Ability to read, interpret, and apply clinic policies and procedures. Ability to identify problems, recommend solutions, and analyze information. Ability to multi-task, establish priorities, and coordinate work activities. Proficiency with Microsoft Office (Word, PowerPoint, Excel) and appropriate practice management software. Work environment and physical requirements
Work performed in a well-lit medical office environment with occasional evening and weekend hours. Physical tasks include sitting most of the day, manual dexterity to operate office equipment, stooping or bending to handle files, and mobility for errands or deliveries. Reasonable accommodations available as needed.
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Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network includes 70+ clinical research sites across the US and Europe focused on GI and hepatology therapies. We empower partner sites with tech-enabled services to drive success and growth by combining clinical trials expertise with AI to accelerate access to novel therapeutics for patients in need. Position purpose
The Nurse Research Coordinator is a specialized research professional working with and under the direction of the Director and Clinical Principal Investigator (PI). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. Responsibilities
Communicate study requirements to all individuals involved in the study. Develop and implement recruitment strategies in accordance with Impact Research and IRB requirements and approvals. Screen subjects for eligibility using protocol specific inclusion and exclusion criteria. Enter participant information and study visit procedures into the Clinical Trial Management System to ensure billing to the appropriate funding source. Maintain adequate inventory of study supplies; when handling investigational drugs/devices, follow sponsor protocol and Impact Research policy on accountability. Complete study documentation and maintain study files per sponsor requirements and Impact Research policies, including consent forms, source documentation, case report forms, and accountability forms. Maintain effective communication with sponsor, research participants, Director and PI during the course of the study. Manage daily study activities, problem-solve, and manage protocol coordination. Collect and report ongoing patient recruitment/enrollment metrics to Director and PI. Arrange secure storage of study documents in accordance with Good Clinical Practice guidelines or as required for the contracted length of time. Protect the rights and welfare of all human research participants in accordance with Federal regulations. Cooperate with compliance and monitoring efforts regarding PHI access, use, and disclosure and report noncompliance as required. Other duties as assigned. Qualifications
Experience:
RN license required; 1-3 years of Clinical Research Coordinating experience preferred. Other Requirements:
None Performance requirements
Knowledge of grammar, spelling, and punctuation. Knowledge of purchasing, budgeting, and inventory control. Skill in taking and transcribing dictation and operating office equipment. Skill in answering the phone and responding to questions. Skill in time management, prioritization, and multitasking. Skill in writing and communicating effectively. Ability to work under pressure and present information clearly. Ability to read, interpret, and apply clinic policies and procedures. Ability to identify problems, recommend solutions, and analyze information. Ability to multi-task, establish priorities, and coordinate work activities. Proficiency with Microsoft Office (Word, PowerPoint, Excel) and appropriate practice management software. Work environment and physical requirements
Work performed in a well-lit medical office environment with occasional evening and weekend hours. Physical tasks include sitting most of the day, manual dexterity to operate office equipment, stooping or bending to handle files, and mobility for errands or deliveries. Reasonable accommodations available as needed.
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