Clinical Research Nurse Resume Samples

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Clinical Research Nurses play a critical role in implementing research projects. Typical duties listed on a Clinical Research Nurse resume are collecting and reviewing clinical data, assisting investigators, screening subjects, and providing support during surgical procedures. Essential qualifications mentioned in a well-written sample resume include scientific terminology knowledge, excellent communication skills, observation spirit, analytical skills, and infection control expertise. Those seeking to secure a Clinical Research Nurse position should be registered nurses and hold at least a Bachelor's Degree in nursing science.

1

Clinical Research Nurse

Coordinated the opening of a 4-bed inpatient Clinical Pharmacology Research Unit

  • Responsible for coordination and implementation of all inpatient and outpatient clinical drug trials.
  • Responsible for protocol review, subject recruitment, adverse event monitoring, ECG monitoring, data acquisition and evaluation.
  • Overhauled study documentation and records keeping. Recognized for excellent documentation during a FDA audit.
  • Coordinated, supervised and successfully completed 7 phase III and IV clinical drug trials involving over 350 subjects.
Candidate Info
10
years in
workforce
3
years
at this job
BS
Nursing
MS
Nursing
2

Clinical Research Nurse Coordinator II

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
Candidate Info
20
years in
workforce
4
years
at this job
AS
Nursing
BS
Nursing
MA
Healthcare Administration
3

Clinical Research Nurse

Reviewed and implemented various phased clinical trials; focused on dissemination of procedural information to staff and participants to ensure consistent and reliable data collection.

  • Obtained Level III position (IV is highest) by successfully achieving standard levels of competencies.
  • Conducted in-services for on-going research/clinical trials (i.e. sleep deprivation and gene therapy projects).
  • Developed sound and effective nurse-to-patient relationships, based on patient assessment and education
  • Served as Charge Nurse, managed daily unit activities as well as handled unexpected emergencies and occurrences. Performed unit-based quality assurance/improvement duties consistent with JCAHO standards. Article published in Medical Surgical Journal on stem cell collection (bone marrow transplant),
Candidate Info
13
years in
workforce
2
years
at this job
BSN
Bachelor of Science in Nursing
Financial And Accounting
Msn
4

Clinical Research Nurse Coordinator

Served as nursing contact for the department of internal medicine investigator-initiated clinical trials.

  • Planned, implemented and evaluated clinical research activities while maintaining a Good Clinical Practice.
  • Performed complex nursing procedures, including patient assessment, specimen collection, intravenous infusions, interpretation and evaluation of patient status and needs. Served as referral to specialists when complex physiological, psychological or psychosocial conditions were noted.
  • Coordinated patient identification, screening, recruitment, consent, enrollment and follow-up for 18 trials while maintaining very low adverse events and morbidity.
  • Maintained confidential files, regulatory documents and completed all case report forms in compliance with NIH, FDA and HIPAA guidelines,
  • Participated all monitored visits.
  • Assisted principal investigators with protocol reviews, IRB applications, annual reports, budget preparation, internal billing and external publication processes.
Candidate Info
10
years in
workforce
1
year
at this job
BS
Nursing
MS
Womens And Childrens Health Nursing
5

Clinical Research Nurse

Assisted in study subject oversight; dosing according to protocol, safety, monitoring, and obtaining informed consent.

  • Observed study protocols, following institutional study compliance and maintained data flow for study coordinators.
  • Supervised staff members such as phlebotomists, medical technicians according to study protocols.
  • Collected and reviewed vital signs, adverse events; performed venipuncture according to study protocols.
  • Maintained study documentation, including completing case report forms, and creating study information material.
  • Assisted with FDA audit of investigational site, study medication, and protocol adherence.
Candidate Info
40
years in
workforce
7
months
at this job
AS
Nursing
Nursing Studies
Medical Abstraction Training
6

Clinical Research Nurse & Study Coordinator

Coordinated over 12 studies researching Chronic Obstructive Pulmonary Disease, including Alpha 1 Antitrypsin Deficiency, Lung Cancer, Asthma Research, Cystic Fibrosis and Inflammatory Markers in Exhaled Breath Condensate.

  • Initiated and completed study protocols and forms for approval by the Institutional Review Board and Clinical Research Center at the university's Shands Hospital and for grants submitted to the National Institute of Health.
  • Wrote nursing protocols and updated and facilitated protocols for bronchoscopies, pulmonary function testing, breath condensate collection, thoracentesis and thoracoscopy.
  • Assisted physicians during procedures such as bronchoscopies, thoracentesis and thorascopy.
  • Tested pulmonary function including spirometry, DLCO, methacoline challenge, hepatic shunt studies, lung volumes by body box and helium frc, arterial puncture for blood gas analysis.
  • Collected samples from study subjects and patients and performed limited laboratory procedures.
  • Recruited patients for studies, administered study drug to patients, and assured patient safety.
Candidate Info
3
years in
workforce
1
year
at this job
Nursing
Emergency Medical Technician
7

Clinical Research Nurse

Coordinated the oncology research activities in the cancer center including the clinical trials with ECOG, SWOG, Northwestern University and its Affiliates, NSABP, NIH and Pharmaceutical Companies like Astra Zeneca, Aventis, and Sanofi-Synthelabo, Inc.

  • Managed the research activities: subjects' recruitment, registration, obtaining of informed consent, data collection, assessment, and follow-up, treatment per protocol, adverse event management and regulatory compliance.
  • Study Coordinator for STAR (Study of Tamoxifen and Raloxifene for Breast Cancer Prevention Trial), SELECT (Selenium and Vitamin E Cancer Prevention Trial) and for all cooperative group trials (prevention and treatment) and pharmaceutical initiated trials.
  • Served as a member of the Silver Cross and St. Joseph Hospital's Institutional Review Board
  • Provide direct supervision to four research assistants
  • Increased subject accrual from 36 to 206 in one year
Candidate Info
44
years in
workforce
1
year
at this job
AS
Nursing
BA
Psychology
Msn/education
8

Clinical Research Nurse

Responsible for managing all aspects of conducting trials, clinical or otherwise; responsible for all aspects of the study to include recruitment, enrollment, ensure adherence to protocol, training of staff, completion of all study visits for eligible participants, GCP, FDA & OSHA regulations. Practiced nursing within the scope of Mississippi RN license to assess, diagnose, plan, implement, & evaluate the nursing care and treatment for the neuroscience patient population.

  • Collaborated with investigators, directors, & sponsors to meet study objectives & resolve problems related to study budget, data, or activities
  • Interacted with study sponsors, regulatory agencies & the IRB on behalf of the study
  • Prepared IRB documents, progress reports, budget, and maintained the regulatory documents
  • Managed data and maintained the research database to ensure confidentiality and data integrity
Candidate Info
15
years in
workforce
4
years
at this job
BS
Nursing
MA
Master of Arts
Ph D
9

Clinical Research Nurse

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
Candidate Info
18
years in
workforce
2
years
at this job
BA
Bachelor of Arts
MA
Master of Arts
Nursing
10

Clinical Research Nurse

Coordinated clinical trials for a major transplant center. Responsibilities included patient recruitment and education, informed consent process, data collection, source documentation, CRF completion and query resolution.

  • Maintained regulatory documents for 18 protocols including all necessary study start-up documents, Institutional Review Board (IRB) application, presentation and submission of annual reports and all correspondence as required.
  • Supervised and completed performance reviews for research assistants and ancillary staff.
  • Presented "Recruitment Strategies" to investigators and coordinators at Hoffmann-La Roche investigators meeting.
Candidate Info
12
years in
workforce
1
year
at this job
AS
Nursing
BSN
Progress

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