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Fortrea Jobs (NOW HIRING)

Instill in all team members Fortrea's commitment to business integrity and quality to meet the client's requirement without error, on time, every time. Financial: * Partner with the CPS Finance ...

$90K - $110K/yr

Clinical Study ICF Writer - US Remote based Fortrea is looking for a confident, seasoned Doc Review Senior Specialist who can work independently while collaborating with globally based team members.

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Fortrea information

What is a Fortrea job?

A Fortrea job typically refers to a position at Fortrea, a global contract research organization (CRO) that provides clinical trial management and drug development services. Employees at Fortrea work in various roles, including clinical research, data management, regulatory affairs, and project management, supporting pharmaceutical and biotech companies. These jobs involve conducting and overseeing clinical studies to ensure compliance with regulatory standards and accelerate the development of new treatments. Fortrea offers opportunities in diverse therapeutic areas and stages of clinical research, making it a key player in the life sciences industry.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Fortrea, and why are they important?

To thrive as a Clinical Research Associate at Fortrea, you need a solid background in life sciences or a related field, relevant clinical research experience, and often a bachelor's degree or higher. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Exceptional attention to detail, strong organizational skills, and effective communication are vital soft skills for managing site relationships and regulatory compliance. These skills ensure the integrity, efficiency, and regulatory adherence of clinical trials, directly impacting patient safety and research outcomes.

What types of projects can I expect to work on as part of the Fortrea team, and how does the organization structure cross-functional collaboration?

As a member of the Fortrea team, you'll likely engage in a variety of clinical research projects, ranging from early-phase trials to late-stage studies for pharmaceutical and biotechnology clients. The work environment is highly collaborative, often involving cross-functional teams that include clinical research associates, project managers, data analysts, and regulatory specialists. Regular meetings and transparent communication channels support effective teamwork and project delivery. You'll have the opportunity to learn from experts across disciplines, which not only enhances project outcomes but also fosters your professional development and exposure to multiple facets of the clinical research process.

What is Fortrea and what do they do?

Fortrea is a global contract research organization (CRO) that provides clinical development and research services to pharmaceutical, biotechnology, and medical device companies. The company specializes in conducting clinical trials, managing data, and supporting regulatory submissions to help bring new therapies and medical products to market. Fortrea's services include clinical trial design, patient recruitment, laboratory testing, and data analysis, making them an essential partner in the drug development process. Their work supports advancements in healthcare by ensuring new treatments are tested safely and efficiently.

What jobs make 5000 a week without a degree?

High-paying jobs that can earn $5,000 a week without a degree include roles such as commercial truck drivers, real estate brokers, sales managers, and certain skilled trades like electricians or plumbers. These positions often require specialized training, certifications, or experience but do not necessarily require a college degree.

What is the difference between Fortrea vs Clinical Research Associate?

AspectFortreaClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRA or RAC are commonRequires a degree in life sciences or healthcare; certifications like CCRA or RAC are often preferred
Work EnvironmentWorks primarily in clinical trial sites, offices, or remotely, supporting multiple projectsWorks at clinical trial sites, monitoring study progress and ensuring compliance
Employer & Industry UsageFortrea is a global contract research organization (CRO) providing clinical trial servicesClinical Research Associates are employed by CROs, pharmaceutical companies, or research institutions

While both roles involve clinical trial oversight, Fortrea is a CRO that employs Clinical Research Associates (CRAs) to manage and monitor clinical studies. CRAs focus on site visits and compliance, whereas Fortrea provides comprehensive trial management services across multiple projects and locations.

What cities are hiring for Fortrea jobs? Cities with the most Fortrea job openings:
What are the most commonly searched types of Fortrea jobs? The most popular types of Fortrea jobs are:
What states have the most Fortrea jobs? States with the most job openings for Fortrea jobs include:
Infographic showing various Fortrea job openings in the United States as of May 2026, with employment types broken down into 97% Full Time, and 3% Part Time. Highlights an 52% Physical, 1% Hybrid, and 47% Remote job distribution.

Director / Senior Manager, Pharmacy - Clinical Research Unit, Madison, WI

Fortrea

Madison, WI • On-site

Full-time

Posted 11 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

Clinical Trials Director / Senior Pharmacy Manager
What if your pharmacy leadership helped new medicines take their first step in human clinical trials?
Fortrea, is one of the world's leading early phase research organizations, delivering first-in-human and early development studies across a global network.
Our Madison, WI Clinical Research Unit brings together clinic and cGMP pharmacy under one roof-offering a modern, integrated environment supported by experienced teams, strong academic partnerships, and access to diverse patient populations.
If Madison is where new medicines begin their journey, this role exists to lead the pharmacy function that makes that possible.
As our next Clinical Trials Director / Senior Pharmacy Manager, you will combine strategic leadership with hands-on operational expertise, leading teams that prepare and deliver investigational medicinal products (IMP) during live clinical trials.
This is a full-time, on-site role in Madison, WI.
WHY IS THIS ROLE DIFFERENT?
This is a rare opportunity to lead pharmacy operations at the front line of first-in-human research.
At Fortrea Madison:
  • Pharmacy, clinic, and quality operate side-by-side in real time.
  • You lead teams preparing IMPs just steps away from dosing.
  • Your decisions directly impact patient safety and study outcomes.

This is pharmacy leadership with immediate, visible impact.
IN THIS ROLE, YOU WILL
Lead and develop a high-performing team
  • Manage Pharmacists and Pharmacy Technicians with clear expectations and standards.
  • Recruit, onboard, and develop talent as the function grows.
  • Foster a culture of accountability, collaboration, and excellence.

Own pharmacy operations for Phase I studies
  • Plan and oversee daily operations supporting active trials.
  • Ensure readiness for early morning dosing and fast-paced execution.
  • Maintain control and consistency in a dynamic environment.

Provide hands-on production leadership
  • Apply and expand expertise in clean room pharmacy operations.
  • Step into operations as needed to support continuity.
  • Lead from the front during complex or time-critical activities.

Ensure GMP and regulatory compliance
  • Own compliance in GMP-aligned, regulated environments.
  • Oversee clean room standards, equipment, and environmental controls.
  • Support inspections and audits in collaboration with Quality teams.

Enable safe first-in-human delivery
  • Ensure accurate preparation of investigational products.
  • Support teams operating at the highest level of clinical risk.
  • Make decisions that directly impact participant safety.

WHAT YOU BRING
Education & Licensing
  • Registered Pharmacist (PharmD) with active state license.
  • We will also consider a Pharmacist with strong management/leadership experience, even if coming from non-clinical research settings, provided there is transferable operational expertise.

Leadership & Industry Experience
  • Demonstrated experience leading, developing, and managing teams.
  • Background in regulated pharmacy, healthcare, or production environments.
  • Ability to scale operations and lead through growth.

Operations & Clean Room Expertise
  • Experience in clean room or controlled production environments (hospital, infusion, institutional, or research).
  • Strong understanding of sterile handling, contamination control, and operational discipline.
  • Ability to operate in highly regulated, quality-driven environments.

Preferred
  • Experience with USP <797> and USP <800> standards.
  • Clean room / sterile compounding background.
  • GMP and/or clinical research (Phase I) experience.

WHY JOIN FORTREA?
If you want to apply your leadership at the point where new medicines first reach humans, this is your opportunity to make a meaningful impact-every single day.
Work Environment:
  • Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
  • Occasional drives to site locations, occasional domestic travel.
  • Exposure to biological fluids.
  • Personal protective equipment required such as protective eyewear, garments and gloves.

Physical Requirements:
  • Ability to work in an upright and /or stationary position for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

Learn more about our EEO & Accommodations request here.