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Job Req ID:  85760

Sr. Research Nurse

We are seeking a Senior Research Nurse who will have responsibilities, directed particularly (but not exclusively) to Sibley Memorial Hospital Radiation Oncology Clinical Trials. This position reports to Principal Investigator(s) and to Oncology Research Nurse Manager.


Specific Duties & Responsibilities:

Project Management

Pre-Study: Anticipates research requirements for designated patient populations

  • May collaborate in development & writing of protocols and consent forms, as appropriate,
  • Collaborates in development and preparation of regulatory documents as appropriate
  • Applies knowledge of study design to evaluate new protocols
  • 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



  • 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
  • Oversees & collaborates in development of study tools including data collection forms, eligibility checklists, preprinted orders, & distribution of the protocol on the Web Library and Internet (where applicable)
  • Assists with preparation of budget for submission and coordinates study sponsor contract designation as appropriate
  • Provides copy of study and pre-printed data forms to Data Management office for review and approval as appropriate
  • Prepares GCRC and PCRU protocol submissions as appropriate
  • Assures receipt of protocol by pharmacy for review & input as appropriate
  • Communicates with coordinating center and provides necessary documentation (i.e., Cvs, 1572, lab licenses, normal values, IRB submissions, etc.) as appropriate
  • Assures compliance with local & national regulatory standards; as appropriate, prepares & submits required regulatory documents
  • Prepares drug data sheets for pharmacy and assures submission of same to CRO/IRB for assigned protocols as appropriate
  • Monitors for and notifies PI of IRB approval/request for further information as appropriate
  • Determines that IRB approval has been received prior to initiation of research activity
  • Represents department at research and protocol initiation meetings
  • Assures that all elements of a trial are in place before opening to accrual
  • Communicates with protocol sponsors, NCI, cooperative group and coordinates plans to address issues with PI


Recruitment & Enrollment: Ensures initial & ongoing eligibility of all subjects for assigned research studies: Same as Level I

  • Collaborates in the development of recruitment strategies to ensure patient accrual within protocol timeframes


Data Collection/Document Maintenance: Ensures collection of pertinent data from internal & external sources & monitors compliance with requirements of assigned clinical trials

  • Applies pharmacological knowledge to assist the investigator in determining adverse event causality & relationship to study drug/procedure
  • Records & documents 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: Evaluates outcomes of clinical trials

  • 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
  • Assumes responsibility for specific QA activities for research teams (i.e., participates in institutional QA process)
  • Participates in sponsor/cooperative group/internal audits/monitoring
  • Assists with development & review of institutional SOPs pertaining to performance of clinical research
  • Maintains records of correspondence of faxes, e-mails, IRB/JCCI submissions, FDA submissions, etc.



  • Independently/collaboratively performs responsibilities of Level I



Patient/Family Education

  • Designs/coordinates educational programs for patients and families relevant to protocols
  • Provides ongoing education to patients and families regarding pertinent clinical trial and clinical management issues


Staff Education

  • Participates in orientation process for new Clinical Research Nurses and Clinical Associates, including mentoring and preceptoring
  • Coordinates and/or presents continuing education/inservice programs for Clinical Research Nurses, Clinical Associates, Data Managers, and others involved in the research process
  • Attends and participates in inservice and external trainings, workshops, conferences, and other relevant programs for professional growth and development



  • Collaborates with other members of the research team in preparing study results for presentation/publication
  • Given opportunities, authors/coauthors manuscripts for publication in the nursing literature and/or presentation at conferences related to areas of expertise
  • Identifies nursing research questions related to protocol populations/issues and, with assistance, collaboration, and appropriate financial support, implements nursing research within departmental priorities
  • Takes advantage of opportunities to make presentations in local community regarding research projects, areas of expertise, etc.


Clinical Practice


  • 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



  • Collaborates with health care team to coordinate and facilitate protocol requirements for assigned clinical trials


Evaluation: Evaluates the effectiveness of nursing care they have planned,

administered, or delegated

  • Evaluates patient=s response to interventions outlined on study protocol; proposes alternative methods to meet individual patient needs
  • 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



  • 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


Clinical Responsibilities

  • Perform clinical duties as assigned


Supervisory Responsibilities:

  • Provides supervision and oversight of Clinical Associates as assigned


Minimum Qualifications (Mandatory):

  • Current licensure in Washington DC as a Registered Nurse is required
  • With a BSN or a non-nursing BA, must have a minimum of three years Oncology Nursing Experience
  • For an RN without a BA/BS, a minimum of five years oncology nursing experience is required
  • Masters Degree is preferred
  • A minimum of three years= direct patient care experience in an Oncology setting is required, with at least one additional year as a Clinical Research Nurse I or equivalent
  • Demonstrated knowledge of computer applications and databases and of personal computer systems is highly desirable


Special Knowledge, Skills & Abilities:

  • Ability to demonstrate knowledge and skills necessary to provide care appropriate to the age of the patients served
  • The individual must demonstrate knowledge of the principles of growth and development over the lifespan and possess the ability to assess data reflective of the patient=s requirements relative to his or her age-specific needs, and to provide the care needed as described in the unit/area/department policies and procedures
  • Knowledge of investigational therapies which require special expertise and clinical care management
  • Highly effective verbal and written communication skills are required


Working Conditions:

  • Possible exposure to communicable diseases, hazardous materials, radiation, and pharmacologic agents. Safety regulations must be followed
  • Work schedules are determined by protocol activity and may demand flexible and/or extended work hours


Classified Title: Sr. Research Nurse
Role/Level/Range: ACRP/04/MF 
Starting Salary Range: $71,510 - $98,410 annually (commensurate with experience)
Employee group: Full Time 
Schedule: M-F 8am-4:30pm 
Exempt Status: Exempt 
Location: Sibley - Washington, DC

Department name: SOM Onc Sibley 
Personnel area: School of Medicine


The successful candidate(s) for this position will be subject to a pre-employment background check.


If you are interested in applying for employment with The Johns Hopkins University and require special assistance or accommodation during any part of the pre-employment process, please contact the Talent Acquisition Office at For TTY users, call via Maryland Relay or dial 711.


Johns Hopkins has mandated COVID-19 and influenza vaccines, as applicable. Exceptions to the COVID and flu vaccine requirements may be provided to individuals for religious beliefs or medical reasons. Requests for an exception must be submitted to the JHU vaccination registry. For additional information, applicants for SOM positions should visit and all other JHU applicants should visit


The following additional provisions may apply, depending on campus. Your recruiter will advise accordingly.


The pre-employment physical for positions in clinical areas, laboratories, working with research subjects, or involving community contact requires documentation of immune status against Rubella (German measles), Rubeola (Measles), Mumps, Varicella (chickenpox), Hepatitis B and documentation of having received the Tdap (Tetanus, diphtheria, pertussis) vaccination. This may include documentation of having two (2) MMR vaccines; two (2) Varicella vaccines; or antibody status to these diseases from laboratory testing. Blood tests for immunities to these diseases are ordinarily included in the pre-employment physical exam except for those employees who provide results of blood tests or immunization documentation from their own health care providers. Any vaccinations required for these diseases will be given at no cost in our Occupational Health office.


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Sibley - Washington, DC