Clinical Research jobs in United States

Explore 416 matching jobs.

ICON plc

Overnight Clinical Research Nurse – PRN

ICON plc

Posted: 10/21/2026
Iovance Biotherapeutics, Inc.

Clinical Trial Manager

Iovance Biotherapeutics, Inc.

Posted: 10/20/2026
University of Pennsylvania Perelman School of Medicine

Clinical Research Project Manager – Hybrid

University of Pennsylvania Perelman School of Medicine

Posted: 10/20/2026
Boehringer Ingelheim

Clinical Trial Manager, Senior – Oncology

Boehringer Ingelheim

Posted: 10/20/2026
Google Cloud Platform
Penn Information Systems & Computing

Clinical Research Project Manager – A-B

Penn Information Systems & Computing

Posted: 10/20/2026
ICON plc

Clinical Research Associate

ICON plc

Posted: 10/20/2026
Syneos Health

Clinical Research Associate

Syneos Health

Posted: 10/20/2026
ICON plc

Senior Clinical Research Associate

ICON plc

Posted: 10/20/2026
IQVIA

Clinical Research Associate – Sponsor Dedicated

IQVIA

Posted: 10/20/2026
Worldwide Clinical Trials

Senior Clinical Research Associate – Psychiatry

Worldwide Clinical Trials

Posted: 10/20/2026
WEP Clinical

Clinical Research Nurse – Home Visits

WEP Clinical

Posted: 10/20/2026
WEP Clinical

Clinical Research Nurse – Home Visits, PRN

WEP Clinical

Posted: 10/20/2026
WEP Clinical

Clinical Research Nurse – Home Visits

WEP Clinical

Posted: 10/20/2026
WEP Clinical

Clinical Research Nurse – Home Visits

WEP Clinical

Posted: 10/20/2026
WEP Clinical

Clinical Research Nurse, Home Visits

WEP Clinical

Posted: 10/20/2026
MSD

Associate Principal Scientist, Clinical Research

MSD

Posted: 10/20/2026
Google Cloud Platform
Thermo Fisher Scientific

Biostatistician II

Thermo Fisher Scientific

Posted: 10/20/2026

Senior Biostatistician

DefinedTalent

Posted: 10/20/2026
Alcanza Clinical Research

Clinical Research Regulatory Specialist

Alcanza Clinical Research

Posted: 10/20/2026
Google Cloud Platform
Worldwide Clinical Trials

Senior Clinical Research Associate – CNS, Psychiatry

Worldwide Clinical Trials

Posted: 10/19/2026
ICON plc

Overnight Clinical Research Nurse – PRN

ICON plc
Posted 10/21/2026part-timeLenexa • Kansas • United StatesMid-LevelSeniorWebsite
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Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in administering investigational products and conducting clinical assessments while ensuring compliance with Good Clinical Practice (GCP) guidelines. Possesses strong communication skills and the ability to collaborate effectively with multidisciplinary teams in a fast-paced clinical research environment.

Highest-signal resume keywords
Registered Nurse (RN) LicenseClinical Research ExperienceGood Clinical Practice (GCP)Medication AdministrationAdverse Event Reporting

About the role

Key responsibilities & impact
  • Administer investigational products according to study protocols and physician orders
  • Monitor research participants during dosing procedures and throughout study participation
  • Identify, assess, document, and report adverse events and other safety findings
  • Perform clinical assessments, vital signs collection, sample collection, and other protocol-required procedures
  • Collaborate with physicians, research staff, and multidisciplinary teams to ensure protocol compliance and participant safety
  • Accurately document study activities and maintain research records in accordance with Good Clinical Practice (GCP) guidelines
  • Educate and support study participants throughout their clinical trial experience
  • Support overnight clinical operations while maintaining a high standard of patient care and data quality

Requirements

What you’ll need
  • Associate's or Bachelor's degree in Nursing or a healthcare-related field
  • Active Registered Nurse (RN) license in good standing
  • Clinical research experience or experience working in a regulated healthcare environment preferred
  • Knowledge of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP)
  • Experience administering medications and assessing patient responses
  • Strong attention to detail and ability to recognize and respond to adverse events
  • Excellent communication and documentation skills
  • Ability to work independently and collaboratively in a fast-paced clinical research setting
  • Ability and willingness to work overnight shifts
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical AssessmentsVital Signs CollectionSample CollectionProtocol ComplianceDocumentation Skills
Soft Skills
Attention to DetailCommunication SkillsCollaborative WorkIndependent WorkPatient Care
Certifications & Qualifications
Associate's or Bachelor's Degree in Nursing
Industry Keywords
Clinical Trial ProcessesRegulatory RequirementsResearch RecordsInvestigational ProductsPatient Safety