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Research Nurse Coordinator - Providence, United States - Lifespan Corporation
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Description
Summary:
Under general supervision coordinates and/or initiates the identification recruitment and follow-up of patients participating in one or more clinical research studies.
Collaborates with physicians/investigators and other members of healthcare team to promote explain and assist in implementation of clinical investigation studies.
Collects data and monitors patients programs assuring adherence to protocols and recommends changes when indicated. Reviews sponsors proposed study budget researches hospital costs to determine adequacy of the budget. Compiles participant data for transmission to the sponsor.Responsibilities:
Coordinates multiple simultaneous clinical research studies within a high degree of independence and using nursing knowledge and experience.
Provides input to physician/investigators regarding the selection of potential new research studies using knowledge of the disease area assessment of availability of patients for the studies and experience from past studies as a benchmark.
Identifies patients meeting criteria for involvement in specific clinical investigation studies assuring all requirements for protocol eligibility have been met.
Facilitates obtaining informed consent of patient following guidelines set forth by Institutional Review Board (IRB). May write consent forms relevant to individual studies. Ensures complete application to the IRB is submitted in the appropriate electronic format.
Establishes study record for each participant abstracting pertinent information from Lifespans electronic record and other medical record documents.
Maintains regular contact with patient and members of healthcare team to monitor adherence to protocol continuously reviewing patient records and data collection sheets alerting physicians when laboratory studies follow-up data and the like are due.
Continuously evaluates patients response to treatment. Reviews data collection sheets abstracting pertinent information to determine response to treatment and to determine any abnormalities or problems.
Alerts appropriate members of the healthcare and/or research team and if appropriate the patients personal physician of any abnormalities or problems associated with patients response to research protocols.
Participates as a member of the research team to provide input regarding revision of protocols assessment and reports of ongoing studies and review of new proposals.
May have direct patient contact to administer drugs to obtain specimens to perform EKGs or other related functions.
Collaborates with Pharmaceutical companies Contract Research Organizations clinical centers and various departments within the institution to evaluate appropriateness and availability of resources equipment availability and staff to establish and conduct research trials.
Participates in professional organization.
Assists with the education of nursing staff and support staff in areas of protocol specific projects.
Other information:
Licensure as Registered Nurse in the State of Rhode Island by the Rhode Island Board of Nursing or licensure as a Registered Nurse in accordance with the Nurse Licensure Compact agreement of the National Council of State Boards of Nursing.
BASIC KNOWLEDGE:
Baccalaureate in Nursing is required including coursework equivalent to a Bachelors level in chemistry biology pharmacology and statistics are required.
A professional level of knowledge in nursing to assess a wide variety of patients for inclusion in studies and to assess response to treatment.
Interpersonal skills to effectively interact with patients physicians research investigators and all levels of personnel within and outside the hospital.
Organizational ability to develop and maintain records and to monitor adherence to protocol for all study patients.
Demonstrates knowledge and skills necessary to provide care to patients throughout the life span with consideration of aging processes human development stages and cultural patterns in each step of the care process.
EXPERIENCE:
At least fives years clinical staff nursing experience to become knowledgeable in the delivery of care to a wide variety of patients and an additional twelve months to become familiar with research projects.
WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS:
SUPERVISORY RESPONSIBILITIES:
None.
Lifespan is an Equal Opportunity / Affirmative Action employer.
All qualified applicants will receive consideration for employment without regard to race color religion sex national origin age ethnicity sexual orientation ancestry genetics gender identity or expression disability protected veteran or marital status.
Lifespan is a VEVRAA Federal Contractor.Location:
The Miriam Hospital
USA:
RI:
Providence
Work Type:
Full Time
Shift:
Shift 1
Union:
Non-Union