Research Coordinator II

Job Details

Are you looking to join a healthcare company that is based on excellence and love? Then this is the position you need to check out!

Christiana Care is one of the country's most dynamic healthcare organizations, centered on improving health outcomes, making high-quality care more accessible, and lowering healthcare costs. Christiana Care includes an extensive network of outpatient services, home health care, urgent care centers, three hospitals (1,299 beds), a free-standing emergency department, a Level I trauma center and a Level III neonatal intensive care unit, a comprehensive stroke center and regional centers of excellence in heart and vascular care, cancer care, and women's health.

It also includes the pioneering Gene Editing Institute and was rated by IDG Computerworld as one of the nation's Best Places to Work in IT. Christiana Care is a nonprofit teaching health system with more than 260 residents and fellows. It is continually ranked by U.S. News & World Report as the Best Hospital. With the unique Care Vio data-powered care coordination service and a focus on population health and value-based care, Christiana Care is shaping the future of health care.

• Full Medical, Dental, Vision, Life Insurance, etc.
• Two retirement planning offerings, including 403(b) with company contributions
• Generous paid time off with annual roll-over and opportunities to cash out
• 12-week paid parental leave
• Incredible Work/Life benefits including annual membership to , access to backup care services for dependents through Care@Work, retirement planning services, financial coaching, fitness and wellness reimbursement, and great discounts through several vendors for hotels, rental cars, theme parks, shows, sporting events, movie tickets and much more!

Christiana Care is searching for a Research Coordinator to provide administrative and operational support for research projects in both outpatient and inpatient settings. Under direct supervision, this position coordinates NICHD Federal grants and other sponsored clinical trials.

• Effectively provides all study related coordination and retention activities for assigned research protocols from study start up through completion.
• Follows study protocols in accordance with Good Clinical Practice (GCP) Guidelines and Standard Operating Procedures (SOP’s).
• Coordinates, evaluates, and performs study procedures as required by the protocol, including screening, recruitment, scheduling, consenting participants, conducting study visits, data collection and recording.
• Informs subjects of any study changes including risks and signs amended informed consents.
• Complete all parameters for protocols competency, including certification quizzes and training sessions, as applicable.
• Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations per study protocol.
• Responsible for the collection and recording of essential data in appropriate files per institutional and regulatory requirements.
• Tracks study progress and assist with activities and submissions to the Institutional Review Board.
• Conducts various assessments and questionnaires, collects, and enters data into electronic databases, such as REDCap, Medrio, Open Clinica, and performs quality assurance on data collected.
• Assists with study orientation and protocol related in-services to research team and clinical staff.
• Serves as a liaison to clinical staff, Principal Investigator(s), sponsor(s), internal and external collaborators.
• Ensure compliance with research protocols and review and audit case report forms for completion and accuracy with source documents.
• Maintains data for queries/audits and…