Under limited direction, as a Research Nurse Coordinator III, you will have primary responsibility for all activities associated with clinical study coordination, including subject recruitment/enrollment, study coordination, data management/integrity, grant expenditure adherence, regulatory compliance, project/study evaluation and subject interfacing. in this role, you will handle the clinical logistics of the study, working in tandem with the Research and/or Clinical Nurse who work to provide hands-on clinical care to the research subject. T he individual filling this dynamic role will lean heavily upon their clinical nursing background to serve as liaisons between nursing staff, the Principal Investigator, other research staff and the study participant. This position serves as a resource to the research staff and provides training, work-review and/or lead direction to junior-level staff.
Responsible for clinical study activities, coordination, adherence to protocols and serves as a liaison between study participants, Principal Investigator (PI), and other research staff.
Provides educational services to research participants and family regarding study participation, participants current clinical condition, and or disease process.
Assesses/documents adverse events as reported by research participants, works closely with PI to document according to department process (grade, attribution, treatment, etc.), reports to regulatory and sponsor as required.
Records research data where assessed or reported by patient (i.e. symptoms of treatment).
Creates and presents education materials to the interdisciplinary team to on study requirements.
Participates in the query and analysis of research data.
Facilitates the education of the interdisciplinary team on study requirements.
Collaborates with the interdisciplinary team to create and communicate a plan of care that allows for safe and effective collection of clinical research data.
Collaborates with the interdisciplinary team to create and communicate a plan of care.
Coordinates research participant study visits.
Triages patient by phone and provides clinical information to the patient.
Recruits of study participants and/or oversees the recruitment of study patients.
Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities and/or has oversight of the research activity.
Coordinates study participant interventions as required and/or has oversight of the research activity.
Serves as a liaison between study participant and PI, Clinical Research Nurse and other research staff.
Prepares data spreadsheets for Investigator and/or department.
Prepares and updates investigation binder.
Completes Case Report Forms.
May prepare IRB submissions.
Assists with data compilation.
May assist with grant proposals, publication preparation, and presentations.
May coordinate grant activities post award through closure (monitoring budgets, compliance, progress reports).
Assists with the education of junior-level staff.
Has general oversight of research portfolio as it pertains to the clinical coordination of the studies.
Serves as a resource to other research staff.
Provides training, work-review and/or lead direction to other junior-level staff.
May process, ship, track or otherwise handle research specimens.
Team Lead/Supervisory/Management Responsibilities :
Establishes effective working relationships with cross-functional team(s) .
Shares knowledge, time and expertise to assist other members of the team .
Represents the company with external constituents .
Teamwork/Customer Relation responsibilities:
Establishes effective working relationships with cross-functional team(s).
Shares knowledge, time and expertise to assist other members of the team.
Represents the company with external constituents.
Providing healthcare for more than 100 years, Cedars-Sinai has evolved into one of the most dynamic and highly renowned medical centers in the world. Along with caring for patients, Cedars-Sinai is a hub for biomedical research and a training center for future physicians and other healthcare professionals. This attracts exceptional talent to Cedars-Sinai, including world-renowned physician-scientists who seek a place where they can both conduct research and see patients--the ideal formula for discovery and its translation into cures. Our patients benefit from access to doctors at the top of their fields, and our researchers have an ideal community in which to study the impact of healthcare challenges, and reflect that knowledge in their research. The greater Los Angeles area in which Cedars-Sinai resides possesses unparalleled cultural and ethnic diversity which offers outstanding opportunities for translational and clinical research... and a dynamic environment for medical education.Although community based, Cedars-Sinai is a major teaching hospital affiliated with the David Geffen School of Medicine at the University of California, Los Angeles (UCLA). Cedars-Sinai has highly competitive graduate medical education programs in more than 50 specialty and subspecialty areas, a graduate program in biomedical sciences and translational medicine, a clinical scholars program directed towards junior physicians with aspirations to become clinical scientists, and post graduate training opportunities.There are more than 250 full-time faculty members at Cedars-Sinai. The voluntary medical staff, comprised of more than 2,200 specialty board-certified or board-qualified physicians, represent all of the specialties and subspecialties and collaborate with full-time medical staff in the teaching responsibilities of the graduate medical education programs.