Nurse Practitioner (NP) for Phase I Site in Dallas, TX

CRO Services LLC

$90K — $120K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Graduate of an accredited Nurse Practitioner program
  • Current NP certification and active licensure
  • Combination of education and relevant experience may be considered
  • Strong English communication skills (spoken and written)
  • 3–5 years of relevant clinical experience

Responsibilities

  • Perform physical examinations, medical histories, and participant assessments as delegated
  • Interact with regulatory bodies to support operational activities
  • Serve as a technical advisor to Clinical Pharmacology teams
  • Participate in clinical feasibility assessments for new study proposals
  • Oversee development and implementation of quality systems for GCP adherence
  • Ensure compliance with FDA, GCP, and ICH regulations
  • Promote and maintain a safe working environment and recommend improvements

Benefits

  • Opportunity to work at a leading Phase I clinical site
  • Role contributes directly to the advancement of clinical pharmacology
  • Collaborative environment with cross-functional teams
  • Access to continuous professional development through training and education
  • Engagement in cutting-edge clinical research initiatives
Full Job Description

Come join Fortrea today as a Nurse Practitioner with our Phase I site based in Dallas, Texas. The NP - Nurse Practitioner provides clinical expertise and serves as a key knowledge resource for the clinical aspects of trials conducted within Clinical Pharmacology. This role supports the execution of clinical studies and may function as a sub-investigator, ensuring high standards of participant safety, data integrity, and regulatory compliance.

Summary of Responsibilities
  • Perform physical examinations, medical histories, and participant assessments as delegated by the Medical Director
  • Interact with regulatory bodies as relevant to operational activities
  • Serve as a technical advisor to Clinical Pharmacology teams and cross-functional partners
  • Support the maintenance and continuous improvement of clinical processes and facilities
  • Participate in clinical feasibility assessments for new study proposals
  • Oversee and contribute to the development and implementation of quality systems to ensure adherence to Good Clinical Practice (GCP)
  • Ensure compliance with FDA, GCP, and ICH regulations
  • Perform routine study-related activities as required
  • Support sponsor visits and interactions in collaboration with operations and client management
  • Promote and maintain a safe working environment; recommend improvements as appropriate
  • Attend investigator meetings as needed
  • Serve as an educational resource, trainer, and mentor to staff
  • Perform additional duties as assigned

Qualifications (Minimum Required)
  • Graduate of an accredited Nurse Practitioner program
  • Current NP certification and active licensure
  • Equivalent combination of education and relevant experience may be considered
  • Strong English communication skills (spoken and written)

Experience (Minimum Required)
  • 3–5 years of relevant clinical experience

Physical Demands / Work Environment
  • Work is performed in a clinical and/or laboratory environment with potential exposure to biological, hazardous, or radioactive materials
  • Ability to distinguish colors and hear clearly
  • Ability to use hands for extended periods (up to 6 hours/day) for clinical and computer-based tasks
  • Ability to stand, walk, bend, and perform repetitive movements for extended periods (up to 6 hours/day)
  • Flexibility to work overtime or weekends as needed

Travel Requirements
  • Occasional travel may be required for investigator meetings, cross-site support, or training

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