Sr. Research Nurse (Oncology)

Johns Hopkins University; Baltimore (MD); On-site; USD 70,000 - 90,000; Full time

Job summary

A prestigious higher education institution in Baltimore seeks a Sr Research Nurse to coordinate and implement clinical trials. The ideal candidate will manage various aspects of study design, oversee documentation, and ensure compliance with regulations. Applicants must be registered nurses with a bachelor's degree in nursing and a minimum of two years of experience. Competitive benefits package offered.

Qualifications

• Registered Nurse licensed in Maryland.
• Minimum of two years experience in a related area.
• Ability to manage multiple projects.

Responsibilities

• Coordinate and implement clinical trials.
• Ensure compliance with regulatory standards.
• Design educational tools for patients and staff.

Skills

Project Management

Regulatory documentation

Pharmacological knowledge

Data collection and analysis

Education

Bachelor's degree in nursing or related discipline

Master's degree preferred

Job description

Overview

Reporting to the Senior Division Manager, Nurse Manager and/or the Lead Research Nurse, we are seeking a Sr Research Nurse who will be responsible for the coordination and implementation of assigned clinical trials within the research program.

Responsibilities

• Project Management
• Pre-study
• Collaborates in development and preparation of regulatory documents as appropriate including consent templating, eligibility checklist, PK/VS/EKG sheets.
• Applies knowledge of study design to evaluate new protocol.s
• Applies knowledge of federal & local regulations when evaluating new protocols.
• Reviews & assesses new protocols for clarity, thoroughness, logistical feasibility, maintaining subject safety, etc.
• Evaluates the impact on & availability of resources for assigned clinical trials.
• Lists & clarifies concerns & questions about new protocols with PI &/or sponsor.
• Proposes & negotiates alternatives to improve protocol implementation.
• Pre-initiation
• Collaborates in the determination of roles & responsibilities of health care team members in the implementation of assigned trials.
• Collaborates in the design of appropriate methods for collection of data required for assigned trials.
• Obtains appropriate data base/electronic data capture training and access.
• Oversees & collaborates in development of study tools including data collection forms, eligibility checklists, Beacon orders, & distribution of the protocol on the Web Library and Internet (where applicable)
• Sets up/assures set up of appropriate research study accounts/ reviews PRA.
• Assures receipt of protocol and other manuals/documents to clinical CORES for review & input as appropriate.
• Assures study documents are uploaded into PRL website for Beacon Treatment Plan development for both new submissions and amendments.
• Assures compliance with local & national regulatory standards; as appropriate, prepares & submits required regulatory documents.
• May participate in drug data sheet development/review/revision.
• Monitors for IRB approval/request for further information as appropriate.
• Determines that IRB approval has been received and study status is Active on CRO protocol library prior to initiation of research activity.
• Represents department at research, investigator and protocol initiation meetings as required.
• Assures that all elements of a trial are in place before opening to accrual.
• Communicates with protocol sponsors, NCI, cooperative group and may coordinate plans to address issues with PI.
• Recruitment & enrollment
• Ensures initial & ongoing eligibility of all subjects for assigned research studies.
• Collaborates in the development of recruitment strategies to ensure patient accrual within protocol timeframes.
• Data collection/Document maintenance
• Applies pharmacological knowledge to assist the investigator in determining adverse event causality & relationship to study drug/procedure.
• Assures accurate recording & documentation of protocol deviations.
• Prepares and submits protocol amendments and revisions as appropriate.
• Demonstrates ability to manage multiple projects at different stages of the clinical research process.
• Demonstrates ability to integrate new clinical trials with current research activity.
• Quality Assurance
• Monitors study team compliance with required study procedures & GCP standards.
• Performs/monitors ongoing data analysis regarding clinical research studies, including toxicities, dose modifications, dose levels, adverse reactions, & response.
• Participates in sponsor/cooperative group/internal audits/monitoring.
• Assures correspondence of faxes, e-mails, IRB/JCCI submissions, FDA submissions, etc. are in the regulatory binder/files.
• Communications
• Communicates effectively with study team members, CORES, clinical staff, patients and families.
• Patient/Family Education
• Designs/coordinates educational education and tools for patients and families relevant to protocols.
• Provides ongoing education to patients and families regarding pertinent clinical trial procedures and management of clinical care.
• Staff Education
• With assistance, coordinates and/or presents continuing education/in-service programs for Clinical Research Nurses, Clinical Nurses, Clinical Associates, Study Coordinators, Research/Standard of care Phlebotomists, and any others involved in the research process.
• Professional Development
• Attends and participates in in-service and external trainings, workshops, conferences, and other relevant programs for professional growth and development.
• Community
• Collaborates with other members of the research team in preparing study results for presentation/publication.
• Clinical Practice
• Planning
• Identifies need and incorporates information from other health care disciplines into clinical research protocol.
• Plans long-term study patient care in relation to identified and potential problems related to assigned research protocols/patient populations.
• Implementation
• Collaborates with health care team to coordinate and facilitate protocol requirements and clinical care for assigned clinical trials.
• Begin to manage multi-modality trials utilizing current treatment modalities.
• Evaluation
• Evaluates the effectiveness of nursing care s/he has planned, administered, or delegated.
• Evaluates patient\'s response to interventions outlined on study protocol.
• Proposes alternative methods to meet individual patient needs and protocol requirements.
• Evaluates effectiveness of nursing care planned on a long-term basis.
• Gives rationale for action/inaction based on scientific principles, practice experience, and internal/external regulations.
• Evaluates patients\' participation in assigned clinical trials and identifies barriers to compliance.
• Plans, proposes and evaluates means to overcome identified barriers to protocol compliance.
• Consultation
• Develops and maintains collaborative relationships with members of other health care disciplines in order to facilitate clinical and research outcomes.
• Provides guidance and direction to other health care professionals (internal and external) in implementation of research protocols.
• Evaluates effectiveness of collaborative role with other health care professionals.

Qualifications

• Minimum Qualifications
• Individual must be a registered Nurse, licensed in the State of Maryland or state where practicing. Bachelor\'s degree in nursing or related discipline required.
• Minimum of two year\'s experience in the specialty or a related area required.
• Additional experience may substitute for bachelor\'s degree and related master\'s degree may be considered in lieu of experience
• Preferred Qualifications
• Master\'s Degree strongly preferred.



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