Instagram
youtube
Facebook

Research Nurse / Open To Rn's, Lpn's Or Paramedics - Dallas, Tx (Weekend Overnight)

0-2 years
Not Disclosed
10 Oct. 7, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Research Nurse / Open to RN's, LPN's or Paramedics (Weekend Overnight)

Location: Dallas, TX
Category: Patient Services
Job ID: 252202
Work Type: Full-time, Weekend Overnight Shift (Friday–Sunday, 6:00 PM – 6:30 AM)
Work Environment: On-site (Clinic-based)
Openings: Multiple


About the Organization

As one of the world’s largest Clinical Research Organizations (CROs), we operate four Early Phase Clinical Research Units across the UK and US. Our mission is to deliver Early Phase clinical trials efficiently and compliantly, partnering with leading pharmaceutical, biotechnology, and medical device companies.

In this role, you will be part of our Clinical Pharmacology Start-Up team, working on Phase I studies that determine the safety, tolerability, and pharmacokinetics of novel drug candidates.

You’ll gain hands-on clinical experience, maintain direct participant interaction, and play a vital role in the development of groundbreaking therapies that improve lives globally.


Position Overview

We are seeking Research Nurses (RN/LPN) and Certified Paramedics to join our weekend overnight team. This position offers a unique opportunity to:

  • Work with diverse therapeutic areas and first-in-human studies

  • Contribute to study initiation and participant safety monitoring

  • Advance your clinical and research skills in a structured, high-quality environment


Key Responsibilities

  • Deliver high-quality participant care using nursing judgment and clinical standards.

  • Respond to medical emergencies following clinical research protocols.

  • Obtain informed consent, educate participants, and administer investigational products.

  • Conduct and document study procedures including:

    • Cannulation

    • Vital signs monitoring

    • ECGs and telemetry

    • Venipuncture

  • Collect and process biological samples, ensuring proper handling and documentation.

  • Accurately record and transcribe source data into Case Report Forms (CRFs).

  • Observe and document adverse events; take appropriate actions.

  • Support start-up activities to ensure studies launch efficiently.

  • Perform other duties as assigned to ensure smooth clinical operations.


Qualifications

Education & Licensure

  • Associate’s or Bachelor’s Degree in Nursing with current state licensure.

  • Equivalent relevant experience may be considered in lieu of degree.

Certifications

  • EMT, Phlebotomy, CMA, or CNA certification preferred.

  • Paramedics must hold current certification.

Experience

  • 0–1 year of nursing or clinical research experience.

  • Exposure to clinical or laboratory environments is beneficial.


Work Environment

  • Clinical/laboratory setting with exposure to biological fluids and electrical office equipment.

  • PPE required (eyewear, gloves, protective garments).

  • Occasional domestic travel or site visits.


Physical Requirements

  • Ability to stand or remain stationary for 10–12 hours per shift.

  • Frequent repetitive hand movements (for equipment operation and sample processing).

  • Occasional bending, stooping, crouching, and twisting.

  • Lift or move objects up to 15–20 lbs (e.g., laptops, supplies).

  • Consistent attendance and flexibility for varied hours as needed.


Key Competencies

  • Thrive in a fast-paced, protocol-driven environment.

  • Adapt quickly to changing priorities and tight timelines.

  • Demonstrate strong team collaboration, communication, and interpersonal skills.

  • Comfortable with electronic data collection systems and technology-based workflows.


Compensation & Benefits

Eligible employees (20+ hours/week) receive comprehensive benefits, including:

  • 🏥 Medical, Dental, Vision, Life, STD/LTD Insurance (multiple carriers)

  • 💰 401(k) Retirement Plan

  • 🏖️ Paid Time Off (PTO)

  • 🏆 Employee Recognition Awards

  • 🌍 Employee Resource Groups (ERGs)


Why Join Us

  • Work on cutting-edge Phase I studies with global impact.

  • Gain hands-on exposure to novel therapeutics and clinical procedures.

  • Build a rewarding career in clinical research with continuous learning and growth.


Equal Opportunity

We are an Equal Opportunity Employer (EEO).
Learn more about our policies or request accommodations via our EEO & Accommodations page.