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Manager Fortrea Jobs (NOW HIRING)

The Senior Clinical Site Director is responsible for the management, administration, and ... Instill in all team members Fortrea's commitment to business integrity and quality to meet the ...

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Manager Fortrea information

What is the difference between Manager Fortrea vs Clinical Project Manager?

AspectManager FortreaClinical Project Manager
CredentialsBachelor's degree, relevant certifications (e.g., PMP)Bachelor's degree, often PMP or similar certifications
Work EnvironmentPharmaceutical/biotech industry, office and site visitsClinical research settings, hospitals, offices
Employer & IndustryFortrea (biotech/pharma)Pharmaceutical companies, CROs
Search & Comparison IntentYesYes

The Manager Fortrea typically oversees multiple projects within the biotech or pharmaceutical industry, focusing on strategic management and team leadership. A Clinical Project Manager primarily manages individual clinical trials, ensuring compliance and timely delivery. While both roles require similar credentials and work in related environments, the Manager Fortrea has a broader scope, often involving higher-level planning and coordination across projects.

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What are the most commonly searched types of Fortrea jobs? The most popular types of Fortrea jobs are:
What states have the most Manager Fortrea jobs? States with the most job openings for Manager Fortrea jobs include:

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

Fortrea

Dallas, TX • On-site

Full-time

Posted 18 days ago


Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

44th of 56 rated research


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

Why Fortrea?
At Fortrea, you'll contribute to advancing clinical development and improving patient outcomes through meaningful work in early-phase research. This role offers a collaborative, fast-paced environment with opportunities to expand your clinical expertise and impact global healthcare innovation.
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