Clinical Research Nurse Job Description
Clinical Research Nurse Duties & Responsibilities
To write an effective clinical research nurse job description, begin by listing detailed duties, responsibilities and expectations. We have included clinical research nurse job description templates that you can modify and use.
Sample responsibilities for this position include:
Clinical Research Nurse Qualifications
Qualifications for a job description may include education, certification, and experience.
Licensing or Certifications for Clinical Research Nurse
List any licenses or certifications required by the position: ACLS, BLS, ACRP, OCN, ONS, CPR, CCRP, CCRC, AHA, BLCS
Education for Clinical Research Nurse
Typically a job would require a certain level of education.
Employers hiring for the clinical research nurse job most commonly would prefer for their future employee to have a relevant degree such as Bachelor's and Associate Degree in Nursing, Education, Science, Communication, Associates, Oncology, Nursing Program, Health, Life Science, Registered Nursing
Skills for Clinical Research Nurse
Desired skills for clinical research nurse include:
Desired experience for clinical research nurse includes:
Clinical Research Nurse Examples
Clinical Research Nurse Job Description
- Adhering to trial protocols and legislation
- Dose investigational product via– oral, topical, inhalation, IM, SC, intranasal, and IV route
- Perform standard nursing care like vital signs, ECG and holter monitoring in a controlled and timed environment
- Collecting trial data
- Participate in development, review and evaluation of study contracts and agreements including identifying resources needed to conduct and evaluate study procedures and data
- Extract data from source documents and complete Case Report Forms (CRF) or database entries
- Aid with administrative duties for the clinical program including but not limited to
- Providing direct patient care involving diagnosis, administration of medications, and performance of tests under the direction of the principal investigator or supervising physician
- Oversees and monitors the well-being and safety of study participants by active assessment by serving as a visible point of contact at all times
- Works with CSM and Training Manager to provide protocol training to the clinical study team, to communicate on-the-spot performance direction
- At least an associate's degree in nursing
- Successful completion of a full 4-year course of study in nursing from an accredited college or university leading to a bachelor's or higher degree
- Showing a flexible attitude with respect to work assignments, new learnings and willingness to work on shift
- Interfacing with the study PIs, Lead Research Coordinator, and Child Psychology Specialist on a regular basis to develop, implement, and monitor adherence to research protocols and standard operating procedures for the research study
- Following up with research participants in accordance with established protocols, which may involve coordinating staffing or scheduling encounters
- Maintain research records, which may include entering data into research data bases
Clinical Research Nurse Job Description
- Assist in the design of recruitment strategies
- Recruit participants according to IRB approved methodologies
- Coordination of visits, Schedule participant visits with support services, perform interviews and clinical assessment to collect data required by the protocol
- Attend and participate in investigator meetings and calls with the sponsors
- Order and receive drug/device supplies
- Oversee proper documentation of close-out as required by grant sponsors including return of unused supplies, reconciliation of test/drug accountability forms, study summary, evaluation of team effort and subject enrollment
- Work involves organizing and executing a phase 3 clinical protocols to compare the safety and immunogenicity of two smallpox vaccines
- Ensure appropriate and accurate documentation of patient care in the medical record and in designated electronic case report forms and specific computer programs
- Advise, perform, and instruct staff, research participants and/or others about protocol-specific procedures and treatments, equipment, policies, adverse medication reactions, and follow-up instructions appropriate to the research study
- Perform and/or assist in participants’ briefings and screenings, to include obtaining of informed consent
- Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree in nursing from an accredited nursing program
- Experience working with toddlers and preschool age children, including performing developmental assessments of and obtaining venous blood samples from toddlers and preschool age children
- Bachelor’s degree in Nursing AND current RN licensure in the state of Maryland
- Must possess basic skills in clinical nursing including drawing blood with butterfly needles and IV catheters
- Must possess and maintain certification to conduct human research such as HIPAA and CITI training
- Based on guidance from Lead Principal Investigator, Site Principal Investigator and Nurse Protocol Coordinator, will update research investigators of relevant issues, concerns, and progress of study
Clinical Research Nurse Job Description
- Assist research investigators in collecting study data and statistics
- Assist PI in submitting annual Continuing Review Reports (CRRs) and annual report for the study
- Write and review Standard Operating Procedures (SOP) and Study Specific Procedures (SSP) and guidelines
- Quality Control (QC) of tracking and filing of all protocol laboratory test results and samples
- QC the preparation of study charts, source documents, labels and laboratory and other test results
- QC of test article (vaccine) accountability
- QC of regulatory study file to include filing of necessary documents per protocol SOP, Food and Drug Administration (FDA) and DA requirements
- Prepare regulatory files and study records for QA audits, monitoring, and assists in responses to audits and monitoring visits
- Reviewing medical records
- Preparing materials for submission to the IRB and participating in protocol development by drafting study protocols and/or reviewing potential protocols to evaluate their effect on standard nursing procedures
- Must possess and maintain a license as a registered nurse in a state or US territory that license nurses
- Have a current BLS certification
- Must be GCP (Good Clinical Practice) trained or willing to complete such training
- Have completed HIPAA training and will comply with proper handling of proprietary information
- None required beyond that described above
- Or Associate’s degree from an accredited institution in Nursing plus 3 years clinical nursing experience
Clinical Research Nurse Job Description
- Perform patient assessment, offer patient education and patient/family support
- Assists with grant and budget preparation
- Develops, implements, and supports research process by assisting investigators in study design, completion of approval process, and management of clinical trials specific to the Peds ID VTEU
- The NIH/DMID VTEU contract for multiple current and upcoming clinical trials requires that nurse coordinators be available to conduct study visits, make appropriate safety assessments, and document all activities as required by each protocol
- Study product administration, obtaining samples (serum, urine, stool) using appropriate techniques, and obtaining individual clinical assessments (EKG, Vital signs, BMI, health history) are critical to the success of DMID sponsored trials
- Mandated training will be required per DMID, NIH, Emory IRB, EHSO and credentialing healthcare entities (EHC, CHOA, Grady)
- Maintain safety and confidentiality of study subjects throughout the study
- Study organization and documentation
- Collection of study data, CRF completion, maintaining source documentation
- Performing patient study visits
- Or LPN or Diploma in Nursing plus 4 years clinical nursing experience
- Involved in external professional organizations
- Preferred oncology nursing experience (at least 1-2 years)
- Preferred research and/or oncology research experience
- Registered nurse with a current, active Colorado license, preferred certification in oncology nursing
- Acts as a professional role model in all aspects of performance
Clinical Research Nurse Job Description
- Coordination of visits, Schedule participant visits with support services, perform interviews and clinical assessment to collect data required by the grant
- Assist adult hematology physicians with sickle cell patients 18-21 transition to their service
- Assist in community programs for patient population including off site workshops, conferences as needed and creating/updating educational materials
- Participate in team meetings and calls with the collaborating physicians and ancillary support staff
- Recruit, screen, enroll, and follow study participants over the course of a study as outlined in assigned cardiovascular research protocols
- Coordinates the implementation of clinical protocols at Northwestern and subsites
- Responsible for ongoing data collection and maintenance of confidential records
- Complete protocol specific nursing assessments for study participants with appropriate documentation in the source record or case report form
- Coordinates with study staff to ensure proper documentation and timing of research-related procedures
- Perform clinical procedures such as IV placement, blood draws from peripheral sites
- Willingness and ability to learn and perform a variety of technical procedures such as drawing blood, processing and harvesting lab specimens, taking vital signs, performing ECGs
- Prior experience in outpatient medical practice with women’s health and/or osteoporosis a plus
- VA RN license
- Minimum three (3) years of practical work experience in healthcare, five (5) years preferred
- While not required, individuals with Advanced Practice Nursing degree will also be strongly considered for this role
- May be expected to sit for CCRP or CCRC certification exam upon eligibility