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Clinical Research Nurse Resume Example

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JC
Jessica Claire
, , 100 Montgomery St. 10th Floor (555) 432-1000, resumesample@example.com
Summary

Nursing RN recent graduate seeking to use attained skills and knowledge to assist your hospital in a nursing role. Proven to competently handle patient care, with the necessary expertise to execute under pressure. Exceptional interpersonal skills, a dedicated worker with strong meaning of commitment. Possess an Associate of Science in Nursing while presently pursuing a Bachelors of Science.

Skills
  • PPE use
  • IV drug therapy management
  • Medication and IV administration
  • Critical thinking
  • Multitasking
  • Communication
  • Laboratory results management
  • Phlebotomy
  • Dispensing oversight
  • Specimen handling
  • Case report management
  • Trial oversight
  • Friendly, positive attitude
  • Reliable and trustworthy
  • Working collaboratively
Experience
03/2021 to Current Clinical Research Nurse Celerion | Orlando, FL,
  • Executed appropriate steps for patient treatment following careful review of physician medical regimen.
  • Administered oral, IV and intra-muscular medications and monitored patient reactions.
  • Coordinated with healthcare team to establish, enact and evaluate patient care plans.
  • Observed strict safety measures, including checking medication dosages before administration to patients.
  • Advocated for patient needs with interdisciplinary team and implemented outlined treatment plans.
  • Maintained strict patient data procedures to comply with HIPAA laws and prevent information breaches.
  • Prepared for upcoming studies by collaborating with program leaders to determine facility and staff needs.
  • Observed patients after administration of designated medication for adverse events.
  • Documented case report forms and collected data for study research logs.
  • Relayed information such as requirements and instructions from clinical team to study participants.
  • Assessed patient conditions, monitored behaviors and updated supervising physicians with observations and concerns.
08/2014 to 03/2021 Clinical Research Coordinator University Of California | Santa Cruz, CA,
  • Participated in regulatory activities and submission by adhering to independent ethics committee and regulatory board.
  • Negotiated investigator budgets for site contracts with support from Administrative Department.
  • Tracked study-specific trial management tools and systems.
  • Performed pre-study, closeout and interim visits to check on study activities.
  • Adhered to standards in all areas, including data collection, research protocols and regulatory reporting.
  • Evaluated proof of eligibility and consent for participants.
  • Obtained informed consent of research subjects or guardians
  • Conducted informed consent presentations and maintained documentation.
  • Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
  • Kept patient care protocols and clinical trial operations in compliance.
  • Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
  • Collected, processed and delivered specimens from trial participants.
  • Reviewed site regulatory binder to check collection procedures and completeness of paperwork.
  • Checked electronic data capturing systems for integrity and compliance.
  • Assessed drug storage conditions and procedures to check adherence to standard protocols.
03/2011 to 08/2014 Medical Coding and Billing Specialist Pacific Dental Services | Winter Park, FL,
  • Read through patient health data, including histories, physician diagnoses and treatments to gain understanding for coding purposes.
  • Carefully coded disease and injury diagnoses, acuity of care and procedures in inpatient setting.
  • Submitted and accurately processed insurance claims with related medical code verifications and assessments.
  • Sought clarification from physicians and other hospital personnel for answers to needed coding interpretations prior to abstracting records.
  • Reviewed and abstracted relevant clinical data from electronic medical records to select appropriate code for procedures.
  • Maintained updated knowledge of coding requirements, which included continuing education and certification renewal.
  • Actively maintained current working knowledge of CPT and ICD-9 coding principles, government regulation, protocols and third party requirements regarding billing.
Education and Training
Expected in Bachelor of Science | Nursing Florida National University, Hialeah, FL GPA:
Expected in 03/2021 Associate of Science | Nursing Carleen Health Institute of South Florida, Plantation, FL, GPA:
Expected in | Billing And Coding Florida Career College - Miami, Miami, FL GPA:
Expected in | Medical Assistant / Phlebotomist Technical Career Institute, Miami, FL GPA:
Languages
English:
Native/ Bilingual
Negotiated:
Spanish:
Native/ Bilingual
Negotiated:
Certifications
  • Registered Nurse, Florida Board of Nursing, License # 9569221
  • Basic Life Support (BLS) Certification
  • CPR certified through American Heart Association

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Resume Overview

School Attended
  • Florida National University
  • Carleen Health Institute of South Florida
  • Florida Career College - Miami
  • Technical Career Institute
Job Titles Held:
  • Clinical Research Nurse
  • Clinical Research Coordinator
  • Medical Coding and Billing Specialist
Degrees
  • Bachelor of Science
  • Associate of Science
  • Some College (No Degree)
  • Some College (No Degree)

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