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Research Nurse Resume Samples
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0-5 years of experience
Conducted Clinical Research which included screening, recruitment and retention of eligible study participants while ensuring compliance with HIPAA, IATA, and FDA regulations
- Responsible for implementing SOPs and improved performance outcome with by 40% in last year
- Budget planning and evaluations, with responsibility for fiscal viability. Budgets on majority of studies returned from a negative to a positive standpoint
- Improved fiscal outcome for department with increased enrollment by 35% by restructuring coordinator’s work plans and assignments
- Supervised clinical staff, including Physicians and nurses, in protocol changes and adherence
- Organized site to promote efficiency and cost effectiveness
0-5 years of experience
- Consistently Exceeded Recruitment Goals
- Accomplished Successful Audits
- Screening, Eligibility, Recruitment and Retention of clinical trial patients
- Accomplished concurrent Successful Audits
- Educated patient and families in pharmaceutical, diagnostic, device and therapy trial protocols in oncology and endocrinology; performed informed consent process.
- Trained and Supervised Employees in EMR with 25% Increase departmental compliancy rates in clinical documentation.
- Conducted education of Information Systems technology and processes; by formulation of staff in-services, via classroom setting, including creation of practical reference materials.
6-10 years of experience
Performed functions of Research Nurse according to protocol in epidemiological study of Mild Cognitive Impairment (MCI)
- Conducted in home interviews including physical examination, neurological exam and psychiatric assessments of geriatric population. Managed case load of an average of 150 study participants
- Performed telephonic interviews that involve in depth health review as required by study protocol
- Administered and interpreted the results of neuropsychological testing that was conducted in the home of the participants
- Participated in recruitment of participants by conducting phone interviews with eligible individuals
- Performed thorough medical record review of participant’s medical records when indicated
- Communicated with other health professionals regarding assessment findings
- Performed venipuncture and processed blood samples according to study protocol
0-5 years of experience
Managed drug clinical trials according to GCP guidelines
- Ensured regulatory compliance of protocol and research documents
- Reported adverse events and protocol deviations to IRB and sponsors as applicable
- Performed data entry on eCRF, verified accuracy of source documents, and resolved queries
- Prepared documents and participated in sponsor monitoring visits and audits
- Maintained and documented on drug accountability logs and other required research logs
6-10 years of experience
Supervised oncology patient care focusing on breast cancer diagnosis and treatment
- Facilitated and coordinated out-patient clinic support
- Featured guest lecturer at the University of Pittsburgh at Johnstown, educating nursing students on the clinical research process
- Appointed member of the Institutional Review Board
- Acted as liaison between clinical and research departments
- Obtained certification by the Society of Clinical Research Associates
0-5 years of experience
Responsible for various aspects of clinical research including: development, management and supervision of clinical programs; site and vendor contract negotiations; organization and presentation at Investigators Meetings, Key Opinion Leader Roundtables and Professional Advisory Board Meetings.
- Collaborated on nine INDs, two Non-US Registrations and eight NDA submissions, six of which were approved.
- Brought two nutraceuticals products to market.
- Provided strategic planning and presentation elements for one FDA Advisory committee meeting leading to product approval.
- Provided expert consultation and presentations for pre-marketed and marketed products.
- Led due diligence on potential and new products through to partnership agreements and beyond, pre- and post-marketing for five compounds (trospium inhaled powder with Alkermes, pagoclone for stuttering with Teva, Sanctura XR with Allergan, Parkinson’s Beverage and other food products with Elan Pharmaceuticals, and Choline sports drink with Boston Sports Supplement with Peak Performance).
- Prepared abstracts for urology, neurology, endocrinology, nephrology and sports health scientific meetings.
- Coordinated manuscript development and submissions to scientific journals.
- Collaborated with sales and marketing development team on pre-marketing strategies of drug products in development; resulted in successful launch of antiobesity, overactive bladder, prostate cancer, bladder cancer and central precocious puberty compounds.
- Directed research trials conducted on the following indications: Antispasticity drug (l-threonine); Parkinson’s Drug (dihydrexidine); Antiobesity Drug (Redux(TM)); Alzheimer’s and Stroke drug (citicoline); Overactive Bladder (Sanctura
6-10 years of experience
- Coordinated all aspects of phase 1-3 HIV trials
- Educated study participants in minimalizing risky behaviors and lifestyle choices
- Implemented two HIV investigator initiated studies (IIS): 88 subjects for 12 US sites; 45 subjects for 9 US sites
- Developed PowerPoint presentations used for protocol training
- Monitored onsite and satellite site data for Investigator Initiated Study protocols to ensure compliance
0-5 years of experience
- Managed, organized and prioritized all activities associated with conducting multiple phase 1, 2 and 3 FDA clinical trials
- Developed protocols and source documents for assigned studies; managed data collection; prepared relevant documentation for submission.
- Communicated with IRB, maintaining and renewing interim reporting requirements.
- Served as liaison between sponsors, investigators, departmental research personnel and other individuals assigned to the study.
- Educated physician and nursing staff on specifics of the protocol, study design and investigational therapeutic agents, procedures and/or techniques specific to assigned study.
- Coordinated the care of research subjects by formulating and continually revising individual care plans to adjust to changes in complex and unstable patients under routine and emergent conditions.
0-5 years of experience
Managed Phase II & III of IRB preparation, regulatory documents, screening and enrollment of patients.
- Performed physical examinations, EKG’s, phlebotomy, and other clinical duties.
- Hired and trained seven research nurses in patient care, document preparation, and Phase II & III requirements.
- Coordinated all phases of clinical studies as well as provided family education and counseling.
0-5 years of experience
Consistently met and exceeded our enrollment goals managing neurology studies such as Alzheimer’s Disease, Multiple Sclerosis, and Parkinson’s Disease, labs, source documents and ECRFs.
- Assisted with Regulatory Affairs ensuring all IRB and sponsor data were submitted appropriately
- Hosted meetings with sponsors, staff, providers, and patients
- Participated in a variety of marketing plans
- Recognized for superior customer satisfaction
6-10 years of experience
- Performed telephone assessments of critically ill patients for entry into phase II-III randomized clinical trials for sepsis
- Prepared clinical vignettes of subject assessments for entry into clinical trials management system
- Contributed written articles for clinical trials newsletters and memos
- Collaborated with developers on design of databases for each trial
- Designed and produced study worksheets, guidelines and training tools for 3 clinical trials
- Presented the company’s role at sponsored investigator meetings
0-5 years of experience
HIV and AIDS Prevention Research Program
- Assisted with the preparation and implementation of standard operating procedures for HIV prevention trials.
- Assured regulatory compliance, assisted with recruitment of eligible participants, screened, interviewed, consented and enrolled participants.
- Assisted with physical examinations, performed venipuncture, and triaged sick calls.
- Performed community outreach, record keeping, made referrals, educated and counseled participants regarding protocol, and completed case report forms.
- Maintained participant’s database and equipment maintenance.
- Assisted with protocol IRB submissions and continuing review.
0-5 years of experience
- Supported implementation of seven study protocols in clinical setting, including identifying and enrolling participants after obtaining informed consent.
- Administered study medication following thorough physical assessment, including managing and documenting participants’ clinical reaction to study medications.
- Provided effective treatment and reversal of anaphylaxis in primarily pediatric population, and maintained clinical study records, case report forms and accurate reporting of adverse events.
- Performed venipuncture/phlebotomy, skin prick tests, spirometry and other procedures per protocol.
- Applied knowledge of Good Clinical Practices, emphasizing subject safety through education and safe environment maintenance, while effectively communicating with subjects, families, and co-workers.
0-5 years of experience
Liaison between sponsor and investigator, sponsor and study participant, and investigator and study participant.
- Screened and enrolled study participants into clinical studies
- Administered study drugs
- Collected data during the study process
- Assessed and completed physical exams of study participants
0-5 years of experience
Enrolling patients in the Thermage eyelid study using unipolar, radio frequency heat
- Assisting with the Thermacool procedure
- Photographing patient’s progress during subsequent office visits
- Keeping detailed records of procedure consents, machine settings, photography and patient progression during the six-month observation period
- Contacting Thermage headquarters for study modifications and submitting those to the appropriate IRB committee at Tristar Corporation for approval
- Administered numbing injections and applied sutures after performing skin biopsies
0-5 years of experience
- Functioned as the sole research coordinator for several Hepatologists and Transplant surgeons in a new Hepatology and Liver Transplant program
- Created comprehensive source documentation for an investigational medical device trial
- Completed case report forms for sponsored clinical trials in a timely manner
- Generated MS Excel spreadsheets for succinct record keeping of budgeted trial expenses
- Coordinated and conducted subject visits
- Kept regulatory documentation, and submitted protocols, addendums, adverse event and safety reports to IRB per institutional regulation
0-5 years of experience
Administered diagnostic interview to research participants in a federally funded genetic study of manic depression.
- Educated subjects and family members on symptoms and treatments for manic-depressive disorder.
- Recruited subjects from local hospitals and mental health facilities.
- Designed, managed and updated databases for research data.
0-5 years of experience
Performed physical assessments of cancer patients on study according to protocol requirements.
- Collected patient assessment data from clinic visits and referred to patients appropriate specialists
- Maintained thorough documentation of patient assessment findings in accordance with clinical standards
- Wrote clinical manuscripts of study findings for publication submission
0-5 years of experience
Maintained accurate and timely documentation
- Acted as a liaison between patient and physician
- Served as patient advocate
- Maintained open lines of communication with physician, patient, and family members
- Educated patient and family members regarding the plan of care
0-5 years of experience
Ensured adherence to established standards and protocols.
- Provided clinical and administrative nursing support for research trials, studies, and projects.
- Assisted in recruitment and screening potential study participants.
- Collected data, assisted in developing data collection systems and compiled reports.
- Completes and corrects case report forms, ensuring accuracy of all records connected with each study with attention to medical events and concomitant medications as well as documentation for each study related event.
0-5 years of experience
Responsible for screening and management of subjects enrolled in Head and Neck Oncology trials.
- Monitored and documented all subject adverse events.
- Patient and family education regarding all aspects of the clinical trial.
- Education and training of staff and infusion nurses on all aspects of each protocol.
- Reviewed all protocols prior to SRC and IRB submission.
- Assisted in training and management of clinical research coordinators.
0-5 years of experience
Intermittent Clinical Research Nurse.
- Provide nursing care and appropriate safety measures to all study participants within the nursing unit
- Responsible for making sure that all protocols are observed and procedures are performed in a time-sensitive
- Administer experimental medication, perform blood draws, set up IVs, administer oxygen, assist with lumbar
- Assess health care needs of the study participants, and plan, implement and evaluate care designed to meet study participants’ needs and safety.
- Work and communicate effectively in a research team to assure that all employees have adequate
- Administer oral medication, intramuscular, and intravenous injections, treatments and other medical procedures as prescribed by the physician.
0-5 years of experience
Recruited patients who met eligibility requirements for participation in research study
- Interviewed participating candidates to gather information necessary for research study
- Communicated findings obtained during interviews to members of the research team
- Utilized various computer programs to document and organize information obtained during patient interviews
0-5 years of experience
Organized Phase I and Phase II oncology research studies per pharmaceutical protocol
- Assisted with managing adverse events and nursing assessments
- Assessed health care needs of patients and reported concerns to Principle Investigators and worked collaboratively
- Managed study patients response to investigational drugs
- Planned, implemented and evaluated care designed to meet patients needs
- Coordinated and scheduled office visits, diagnostics and labs
- Performed comprehensive documentation via EMR system
- Trained and supervised staff of accurate procedures, etc.
- Drug Accountability for study drug
- Performed IV access, port acces, peripheral, etc as needed
6-10 years of experience
Assisted the PI with determining feasibility for trials and determining initial budgets.
- Evaluated and generated the initial study calendars and schedule templates for trials
- Evaluated patients and assisted in identifying patients who were eligible for trials.
- Explained the trial to the patients and obtained consent.
- Followed the patients independently at their clinic visits.
- Reported AE’s and SAE’s to the proper reporting agencies.
- Participated in site visits and monitoring visits throughout the trial.
- Successfully managed 4 to 5 phase one to three clinical trial at the same time.
- Followed non study patients in clinic with a physician.
- Developed plans of care for treatment patients.
- Educated patients new to receiving chemotherapy and saw them at each visit to reinforce teaching.
6-10 years of experience
Screened potential research subjects
- Complied with GCP and FDA regulations
- Provided source and case report form documentation and database management
- Completed Investigational New Drug safety reporting
- Maintained study drug inventory and completed research pharmacy audits
0-5 years of experience
Coordinated multiple phase IV and PI initiated clinical trials including a variety of drug and device trials. Reported directly to Principal Investigator and managed one direct report.
- Submitted all regulatory submissions, follow-ups, and study startup for all trials
- Assisted PI in ICF/ protocol writing and revision of PI initiated study
- Creation and revision of databases and logs to maximize screening and enrolling efforts
- Worked with all investigators to create new methods for identifying eligible patients to increase enrollment
6-10 years of experience
- Prepared research protocols and informed consents for review by Institutional Review Board
- Screened new patients in clinic for eligibility for research protocols
- Presented protocol and informed consent to patients
- Coordinated all pre-study screening tests with clinic
- Managed patient care with treating physician according to protocol guidelines
- Educated physicians, clinic staff, and patients on protocol requirements
- Completed case reports forms
0-5 years of experience
- Robert Wood Johnson Society, 24-month term “Nursing-Pharmacy Collaboration on Medication Reconciliation-A Novel Approach to Information Management”.
- Collected data from medicine service patients on home medication lists and entered medications on POE software under Home Medication List.
- Researched patients’ home medication lists from EPR, previous discharge summaries on POE, and MMF.
- Identified medication discrepancies using consented-patient information from pre-admission, admission, and discharge.
- Developed teaching tools to assist patients with medication compliance and adherence such as medication calendars, wallet-size medication cards, and medication identification.
- Directed patients with financial need to appropriate team members to prevent omission of medication and ensure adherence and compliance.
- Principal Investigator Linda Costa PhD.
0-5 years of experience
- Charge nurse: supervised two inpatient research units during both day and night shifts
- In-depth knowledge of active protocols; ensured nursing team competence
- Patient education and medication administration based on multiple study schedules
- IV starts, telemetry, specimen collection, EKGs, quality management
- Assisted with randomization, spinal catheter insertion, and blood patches
- Utilized nursing process to meet participants’ safety needs and plan of care
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[Research Nurse]
Last edited by: Gabriela Barcenas, CPRW, Content Writer II -
Gabriela Barcenas
CPRW, Content Writer IIGabriela is a Certified Professional Resume Writer (CPRW) and career adviser. With 10 years of digital media experience and five years of resume writing expertise, her publication history includes fashion, education, travel, social justice, equitable design and career advice.
