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Clinical Research Nurse Resume Samples
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0-5 years of experience
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.
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
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),
0-5 years of experience
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.
0-5 years of experience
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.
0-5 years of experience
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.
0-5 years of experience
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
0-5 years of experience
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
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
0-5 years of experience
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.
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
6-10 years of experience
- Initiated division’s clinical research program of Sponsored Drug studies and Investigator-initiated research projects (Abbott Labs, Amgen, Immunex).
- Effective set-up of trials to meet the needs of small Investigator group (5 MDs). Oriented new Fellows to clinical research processes.
- Performed efficient and organized study visits; data collection, phlebotomy, self-injection education, etc.
- Prepared IRB reports; managed one assistant; collaborated with software programmer to develop division’s research database (MS Access).
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
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
- Coordinated clinical research programs in both the inpatient and outpatient settings.
- Worked in a diverse role as a clinician, educator, and researcher.
- Maintained collaborative relationships with physicians, nurses, and other healthcare providers.
- Provided patient and family education on disease processes, treatments, and medications.
- Reviewed medical records to assure proper enrollment into clinical trials and data collection.
- Administered therapeutic interventions, monitored patients, and collected data that maintained protocol adherence.
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
Successfully coordinated the cardiovascular clinical research program, including device and drug studies, registry management, compassionate-use protocols, HDE programs, and investigated initiated research.
- Provided direct nursing care, protocol administration, and performed all aspects of IRB, budgeting, adverse event reporting, and regulatory activities.
- Coordinated multiple clinical and operational service lines to ensure protocol compliance.
- Served as an IRB member and conducted on-site study audits for regulatory compliance.
0-5 years of experience
Supervised organization and administration of all aspects of clinical studies including recruitment and enrollment of all volunteer study patients and maintenance of study progress.
- Actively participated in all special protocols and test interpretations and results.
- Responsible for nursing in-service training regarding implementation of protocols.
- Counseled patients regarding protocols, test interpretations and results.
- Assisted physicians with examinations and diagnostic procedures.
- Independently conducted phlebotomy and inseminations.
0-5 years of experience
Hematology/ Oncology/ Transplant
- Promoted leadership as unit charge nurse and unit Code Blue trainer
- Administered blood products, chemotherapy/biotherapy agents, investigational agents, factor products and stem cells per protocol
- Resourced staff on IV insertion and phlebotomy
- Oriented newly hired staff nurses and mentored nursing students
- Educated patients on research protocols and informed consent
- Served as primary nurse to Stem cell and bone marrow transplant patients
0-5 years of experience
Acted as part of a team of clinical professionals in the multistage development of pharmaceuticals for the treatment of various ophthalmic disorders
- Conducted physical exams to monitor the safety of patients participating in investigational drug trials
- Utilized clinical judgment and physical assessment skills to determine if patients met criteria to participate as well as monitored for adverse events throughout the trials
- Made appropriate referrals if medical conditions were identified during physical examinations
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
- 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
- Administered medications via different routes: oral, subcutaneous, intramuscular, dermal, inhalation, topical, and rectal
- Performed venipunctures and IV insertions
- Performed and assessed ECG’s, vital signs, telemetry and spirometry
- Assessed and intervened during adverse reaction
0-5 years of experience
Analyzed highly complex data gathered on clinical research studies and interpreted clinical research data. Assured all protocol procedures were approved and followed.
- Ensured clinical trials and studies were run according to specific protocols and regulatory procedures.
- In addition to providing and coordinating clinical care, responsibilities also included a central role in assuring participant safety, ongoing maintenance of informed consent, maintaining integrity of protocol implementation, providing accuracy in data collection.
- Responsibilities also included recording collected data into computer data base in electronic worksheet form.
- Thoroughly reading and understanding study protocols and ensuring protocol is strictly followed by physician as well as participant
- Demonstrated exceptional attention to detail and accuracy, also demonstrated leadership potential.
0-5 years of experience
Cared for 35 patients daily
- Managed a staff of 6 certified nursing assistants
- Administered medication (pill, IV, transdermal, injections, and insulin) daily
- Verified MAR’S daily
- Provided tracheostomy care daily
- Arranged EMS transportation as needed for patients
6-10 years of experience
Coordinated research projects in compliance with IRB regulations
- Collected data and perform clinical assessment according to protocols
- Facilitated patient enrollment and participation in studies
- Prepared, interacted, and supported investigators and clinical monitors during routine visits and audits
0-5 years of experience
- Provided patient education regarding medications, disease management, and lifestyle interventions.
- Managed Phase II and III pharmacology clinical trials in congestive heart failure and hyperlipidemia.
- Authored written protocol summaries and informed consent forms for IRB submission.
- Worked with monitors from pharmaceutical companies and clinical research organizations to review source documents and remote data entry information for accuracy to ensure compliance with
- Monitored adverse events and authored reports for study sponsor and IRB submission.
- Recruited and enrolled study participants based on protocol criteria.
0-5 years of experience
Managed all clinical research projects
- Coordinated clinical trials from phone screening, to randomization, to study completion
- Reviewed study protocols and investigator brochures, assisted is IRB application
- Reviewed and maintained regulatory documents and IRB correspondence
- Maintained tracking system for each study, for the effective communication and submission of required documents to the IRB
- Reviewed and participated in the determination of eligibility and recruitment of candidates for study participation
- Coordinated research-related activities, such as study visits and follow up blood work/buccal swabs
0-5 years of experience
- Coordinate care for patient’s on Phase II-III oncology research protocols
- Instituted ways to increase physician awareness of active research protocols
- Increased patient accruals to research protocols by 75%
0-5 years of experience
Support the PPD Dental Clinic in the overall conduct of multiple, ongoing clinical trials involving oral surgery patients in an in-patient setting, ensuring patient safety and cooperation during the study process.
- Ability to function with multiple types of individuals and work in a team environment while maintaining a positive attitude
- Exhibit motivation and dedication by providing the highest quality of care to each patient
- Strong planning and organizational capabilities to manage multiple tasks and study groups at one time
- Willingness and ability to administer investigational drugs including oral, intravenous, topical, and other approved methods of dosing
- Willingness and ability to perform a variety of technical procedures such as drawing blood, processing and harvesting lab specimens, taking vital signs, performing ECGs, etc.
- Excellent verbal and written communication skills
0-5 years of experience
Coordinated clinical research studies within the hospital setting
- Recruited patients for clinical studies
- Organized and maintained research data
- Served as liaison between research staff, patients and IRB
- Ensured compliance with good clinical practice
6-10 years of experience
Works collaboratively with principal investigators, research coordinators, and clinical staff to ensure efficient implementation of research protocol procedures cohesive to IRB regulations
- Functions as a CITI trained research nurse liaison assuring new research protocols are in alignment with IRB regulatory standards
- Knowledgeable of laboratory specimen processing with compliance to CAP CLIA standards
- Preceptor to new staff and mentored nursing students
- Provides direct patient care to research subjects and to overflow patients
- Interprofessional committee member to enhance employee engagement in unit activities that impact study team and subject relationships with the clinical staff
0-5 years of experience
Provide inpatient and post-surgical nursing care to patients with various genetic, endocrine and respiratory disorders.
- Manage patients in various research protocol through administering research study medications, collecting research samples, assisting with unit procedures, and obtaining and documenting essential data used by researchers within the National Institute of Diabetes and Digestive and Kidney Diseases, National Heart, Lung, and Blood Institute, and the National Institute of Child Health and Human Development.
- Serve as charge nurse during various shifts and periodically floats to various units throughout the hospital.
- Provided comprehensive health care to adult patients with hematological cancers, and various other medical disorders.
- Assessed and administered medications, blood products, and chemotherapy to patients with chronic and acute respiratory disorders within the pulmonary stepdown (PCU)
- Obtained and interpreted lab values
- Started and maintained central venous and intervenous access, and providing safe and effective nursing care to a typical patient load of 4-6 patients.
- Functioned as a vital team member to the nursing and medical staff by serving as a nursing preceptor to new, incoming nurses to the unit
0-5 years of experience
- Administered and assessed patient status during medication administration.
- Maintained aseptic and sterile technique during procedures.
- Performed ECGs, monitored vital signs, and performed injection site assessments.
- Inserted IVs, performed blood withdrawal and processed lab samples.
0-5 years of experience
Assisted medical directors of Outpatient Clinic with development of Tele-monitoring program, including writing manual for healthcare providers and patients use, setting monitors up in trial patients home and instructing patient and family on use of machine.
- Wrote patient and staff educational materials, including manual for all post kidney and Kidney/Pancreas transplant patients. Completed a three hundred page teaching manual for patients and families reviewing surgical healing, medications, diet, activity level etc.
- Provided patient education to patients in outpatient setting. Reviewed medications, changes in medication, monitoring care at home as well as signs and symptoms of complications post transplant.
- Managed research protocols – Identified appropriate patient population, communicated effectively with medical and clinic staff the purpose, implications, protocol and effectiveness of individual research protocols
- Assisted in outpatient clinic patient care, including routine blood drawing, review of medications, doses, frequency and side effects with patients and family members
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
Well-versed in developing and implementing procedures, data and quality assurance standards for monitoring components of studies
- Implemented research protocols including screening and enrollment
- Administered medication when necessary
- Maintained patient records
- Validated data to achieve goals of research projects
- Liaised between physicians, staff, patients and external agencies
- CITI certified for human subjects
6-10 years of experience
Multi-study NIH research institute specializing in cardiac and pulmonary research. Researcher on CAST, SOLVD and TIMI cardiac studies. CASS registry follow-up
- #1 Recruitment site in the United States for CAST and SOLVD cardiac studies
- Detailed chart review and screening, patient interview and recruitment, data collection and computer entry.
- Assisted physicians in Pulmonary Clinic and triaged patient phone calls
- Specialized in Asthma education and smoking cessation in pulmonary clinic
0-5 years of experience
National Heart Blood and Lung Institute (NHLBI)
- Clinical trial facilitation, implementation, and publication
- Conducted clinical trials according to ICH, GCP guidelines
- Prepared and developed SOPs for the clinical trial department
- Exemplary patient recruitment
- Case Report Form creation
- Scientific Review Board and Institutional Review Board submission
- Organized and coordinated weekly clinical treatment of 500 sickle cell patients
- Coordinated physician’s clinic and collaboration between departments
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
0-5 years of experience
Managing and coordinating care for active and follow up research patients at two clinical sites, including all stages from screening to end of treatment, as well as follow up.
- Experience includes phase Ib to phase IV clinical trials, both pharmaceutical and cooperative.
- Clinical indications include bladder cancer, prostate cancer, lung cancer, pancreatic cancer, colorectal cancer, breast cancer, ovarian cancer, sarcoma, lymphoma, cancer anorexia-cachexia syndrome, etc.
- Ensuring proper protocol execution and compliance for numerous study subjects by following strict protocol and federal guidelines.
- Acting as a liason between investigators and sponsor companies.
- Reviewing study protocols for clinical effectiveness prior to study start-up.
0-5 years of experience
Compiled all required documentation for the local Institutional Regulatory Board and the Food and Drug Administration application process.
- Coordinated all patient related activities; venipuncture, processing and shipment of specimens; maintenance of laboratory reports; transcription of data and recording of adverse events in accordance with FDA standards; medication dispensing and accountability.
- Provided on-going assistance with Telehealth research project.
- Provided on-going assistance with recruitment activities for the Research Center.
0-5 years of experience
- Conducted clinical trials in compliance with protocol, GCP guidelines and FDA regulations
- Facilitated periodic monitoring visits
- Conducted consent discussion and obtained informed consent
- Administered investigational drugs, maintained records for the receipt, dosing, administration and accountability of investigational product
- Responsible for the completion and/or correction of source documents
- Verified and responded to queries
- Participated in investigator meetings, sponsor initiation visits, protocol reviews, and development of source documents
- Assessed, documented, and managed AEs and SAEs
0-5 years of experience
Liaised between PI, medical staff and patients for appropriate patient care.
- Educated patients regarding Pre and Post radiation treatment care.
- Accessed surgical sites and perform nursing functions to care for wounds.
- Obtained IC prior to patients starting on protocols.
- Coordinated and determine appropriate protocols based upon eligibility
- Prepared and cared for patients undergoing Gamma Knife radiation.
0-5 years of experience
Organize, coordinate and implement clinical trials in the Division of Infectious Diseases and HIV Medicine.
- Perform clinical duties as indicated by individual protocol requirements
- Maintain and submit accurate data for submission to monitoring agency
- Recruit and screen all potential and physician referred patients for eligibility requirements
- Review clinical research protocols and make change recommendations as needed
- Maintained excellent compliance with all institutional and sponsor-related regulatory procedures
0-5 years of experience
Screen and enroll patients in current investigator initiated and sponsored studies
- Submit and maintain new studies, modifications, reports, close outs and any other regulatory needs to the Institutional Review Board and the Office of Research Administration at Florida Hospital as well as any other entities that may pertain to each study, respectively
- Develop and maintain databases in excel for each investigator initiated study
- Stay abreast of current research guidelines and inform physicians of any changes
- Educate advanced fellows on International Conference on Harmonization/ Good Clinical Practice guidelines
- Create and manage budgets and invoicing for Sponsored drug and device studies
- Submit for Medicare preapproval for any investigative devices
0-5 years of experience
I work with the Hematology physicians on Phase I and Phase II clinical trials pharmaceutical and industry.
- I screen patients for studies and enroll patients on studies.
- I am familiar with all types of data submission.
- I have hands on experience with patients explaining studies to patients and what a study will entail.
- I schedule patients for test, procedures, physician visits, labs and etc per protocol.
- I am familiar with all aspects of a study (adverse events, minor deviations, major deviations, serious adverse events, study calendar and etc.)
- I am a coordinator over at least 10 studies.
0-5 years of experience
- Clinical Research Coordinator for urology practice that conducted pharmaceutical trials Phases 2 through 4.
- Responsible for study recruitment, regulatory documentation management, IRB interaction, enrolling subjects into clinical trials, obtaining consents, subject recruitment, subject screening, CRF completion, collecting laboratory specimens and documenting adverse events.
- Performed CPT coding for all hospital services i.e. surgeries, consults, E&M visits.
- Office manager from September 1996 through September 1999
0-5 years of experience
Responsible for coordination of patient care activities and participation in the conduction of studies for patients enrolled in clinical studies at the Regional Care Network, while maintaining compliance with all regulatory, institutional, and departmental requirements.
- Perform assessments, correlate research data and interact with protocol sponsors, regulatory agencies and the Primary Research Study Staff at MSKCC main campus locations.
- Perform data collection, data entry and patient recruitment.
- Investigator on Therapeutic Research Protocol 12-204: Phase II Study to Evaluate the Safety and Efficacy of IZN-6N4 for the Prevention of Chemo-Radiation-Induced Oral Mucositis in Patients with Head and Neck Cancer.
- Consenting Professional on Specimen Banking Research Protocol 06-107: Storage and Research Use of Human Biospecimens.
0-5 years of experience
- Verify subject eligibility based on specific criteria requirements; run 2-3 studies (50-120 subjects) simultaneously.
- Observe drug preparation in pharmacy; confirm correct medications and dosages prior to administration.
- Continuously monitor subjects; obtain biological specimen samples, EKGs and vital signs to assess changes.
- Document adverse events and treat as directed by Principal Investigator; respond to all emergencies.
- Member of the Emergency Control Plan Committee; maintain the emergency response cart.
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[Clinical 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.
