LPN Research Coordinator

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services.

By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

• Perform quality work within deadlines with or without direct supervision.
• Interact professionally with other employees, customers and suppliers.
• Work effectively as a team contributor on all assignments.
• Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations.

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.

• Communicate study requirements to all individuals involved in the study.
• Develop and implement recruitment strategies in accordance with GI Alliance 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 appropriate funding source.
• Maintain adequate inventory of study supplies. When handling investigational drugs/devices, follow the sponsor protocol and/or GI Alliance RESEARCH Policy on Investigational Drug/Device Accountability.
• Complete study documentation and maintain study files in accordance with sponsor requirements and GI Alliance RESEARCH policies and procedures.
• Maintain effective and ongoing communication with sponsor, research participants, Director, and PI during the study.
• Manage day-to-day study activities including problem solving, communication, and protocol management.
• Collect and report ongoing patient recruitment/enrollment metrics to Director and PI.
• Arrange secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer.
• Protect the rights and welfare of all human research participants in accordance with Federal regulations.
• Cooperate with GI Alliance RESEARCH compliance and monitoring efforts regarding access, use, and disclosure of PHI and report instances of noncompliance to the appropriate compliance office.
• Other duties as assigned.

Experience:

• LVN-LNP license required.
• 1–3 years of Clinical Research Coordinating experience preferred.

None

• 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.