Research Nurse – Clinical Trials focus, Pharmaceutical Industry

🏢 IQVIA📍 Tallahassee, FL, United States💼 Full-Time💻 On-site🏭 Pharmaceuticals and Clinical Research💰 65000-85000 per year

About the Company

IQVIA (NYSE: IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human science and data science to make a bigger impact on global health. Our work in clinical trials helps bring new medications and therapies to patients worldwide, improving health outcomes and quality of life. Join a team dedicated to innovation, patient safety, and scientific excellence.

Job Description

We are seeking a highly motivated and detail-oriented Research Nurse to join our clinical trials team in Tallahassee, FL. In this critical role, you will be instrumental in the execution of phase I-IV clinical research studies, ensuring the highest standards of patient care, data integrity, and regulatory compliance. You will work closely with investigators, study coordinators, and pharmaceutical sponsors to manage patient visits, administer study interventions, and meticulously document all study-related activities. This position offers an exciting opportunity to contribute to cutting-edge medical advancements in a dynamic pharmaceutical industry setting.

Key Responsibilities

  • Perform comprehensive nursing assessments of study participants according to protocol requirements.
  • Administer investigational medicinal products and perform venipuncture, ECGs, and other clinical procedures.
  • Monitor participants for adverse events, document findings, and report to the investigator and sponsor as required.
  • Educate participants and their families about the study protocol, procedures, and potential risks/benefits.
  • Ensure accurate and timely collection, recording, and reporting of clinical data in case report forms (CRFs) or electronic data capture (EDC) systems.
  • Maintain strict adherence to study protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements (e.g., FDA regulations).
  • Assist with participant recruitment, screening, and enrollment processes.
  • Manage study drug accountability and ensure proper storage and dispensation.
  • Collaborate effectively with the research team, investigators, and sponsors.
  • Participate in site monitoring visits and audits, providing necessary documentation and support.

Required Skills

  • Active Registered Nurse (RN) license in the state of Florida.
  • Minimum of 2 years of clinical nursing experience, preferably in an acute care setting.
  • Strong understanding of medical terminology, anatomy, physiology, and pharmacology.
  • Excellent written and verbal communication skills.
  • Proficiency in clinical assessment, venipuncture, and medication administration.
  • Ability to work independently and as part of a multidisciplinary team.
  • Exceptional attention to detail and organizational skills.
  • Basic computer proficiency, including experience with electronic health records (EHR) and Microsoft Office Suite.

Preferred Qualifications

  • Bachelor of Science in Nursing (BSN).
  • Previous experience in clinical research or pharmaceutical trials.
  • Knowledge of Good Clinical Practice (GCP) guidelines and FDA regulations.
  • Certification in Clinical Research (e.g., CCRC, CCRP).

Perks & Benefits

  • Comprehensive medical, dental, and vision insurance.
  • Generous paid time off (PTO) and company holidays.
  • 401(k) retirement plan with company match.
  • Tuition reimbursement and professional development opportunities.
  • Employee assistance program.
  • Life and disability insurance.

How to Apply

If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:

  • An up-to-date Resume or CV
  • A brief cover letter summarizing your experience and motivation

Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.

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