76082BRJob Posting Title:Clinical Research CoordinatorDepartment:Computational Health Informatics ProgramAutoReqId:76082BRStatus:Full-TimeStandard Hours per Week:40 Job Posting Category:ResearchJob Posting Description: We are seeking a Research Coordinator to join PrecisionLink, a major research initiative at Boston Children’s Hospital. The aim of this initiative is to link research and clinical missions at our hospital by establishing the technology, policies, and workflows to engage our patients in research, and treating each visit as an opportunity for patients to contribute to our scientific knowledge. PrecisionLink has built a knowledge base of linked genomic and phenotypic patient data for use in research, as well as in clinical care.

The position is in the Boston Children’s Hospital Informatics Program ( www.chip.org ), a world-leading multidisciplinary applied research and education program advancing biomedical science, health care delivery, and public health. The position will provide opportunities to work in a variety of clinical and research environments.

The Research Study Coordinator will be responsible for:

• Working with team leads to develop strategies for recruitment of study participants in different clinical settings.

• Training of research study assistants on project workflows and participant enrollment.

• Recruiting study participants for enrollment in both inpatient and outpatient clinical settings.

• Coordinating daily operations of the study and organizing study procedures; developing workflows to enhance efficiency.

• Corresponding with study participants via virtual platforms.

• Participating in all aspects of data management , including collection, coding, and entry of study data; conducting periodic testing of data validity, and identifying and resolving errors or discrepancies.

• Preparing data summaries and reports for internal and external audiences, including tables, charts, and graphs.

• Maintaining regulatory binders, case report forms, source documents, and other regulatory study documents; monitoring the occurrence of clinical adverse events.

• Ensuring compliance with goals and objectives of research protocols and with state and federal regulatory guidelines.

  Qualifications:

• Bachelor's degree with three years of related experience. Alternatively, a Master's degree and one year of relevant work experience.

• Prior experience in clinical research is highly desired.

• Analytical skills to synthesize and summarize data for presentations and to guide protocol development.

• Effective communication skills to interact with parents and study participants, including explaining research studies, obtaining informed consent, and addressing questions from clinicians and researchers.

Office/Site Location:BostonRegular, Temporary, Per Diem:Regular Remote Eligibility :Part Remote/Hybrid