Consulting Intern

Company Overview:

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of drug development, patient access and technology solutions across more than 20 therapeutic areas. With over 15,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Fortrea is driving the innovation that advances healthcare solutions.

Fortrea brings together the innovation and agility of a new, global CRO backed by 30 years of experience to provide our customers comprehensive drug development and commercialization services for biopharmaceutical products.

By merging the energy and agility of a new company with three decades of experience and unparalleled clinical data, Fortrea partners with emerging and large biopharma, medical device, and diagnostic companies to drive healthcare innovation and improve the lives of patients worldwide through:

• Consulting and Regulatory Services
• Clinical Development
• Clinical Pharmacology
• Therapeutic Indications
• Enabling Technologies
• Full and Functional Service Provider Models

Job Overview:

We are excited to offer a 12-week remote paid Regulatory Strategy Internship opportunity for individuals interested in gaining hands-on experience within our Regulatory Strategy and Product Development Consulting Department. As an intern, this role will allow you to work closely with our Regulatory Strategy Consulting Team to support regulatory strategy development , consulting frameworks, and innovative solutions for clients in the healthcare and biopharma industries.

Internship Assignment Summary:

• Assist the Regulatory Consulting team in the development and analysis of client project deliverables.
• Research emerging trends, and regulatory frameworks to support client solutions.
• Collaborate on projects involving regulatory strategy design for product development, patient access, and market entry.
• Contribute to data analysis, reporting, and presentation development for clients and leadership teams.
• Support internal project management tasks, including documentation, meeting coordination, and solution tracking.

Education/Qualification/Skills:

• Current enrollment in a Bachelor's or Master's program with a focus on Healthcare, Clinical Research, Life Sciences, Public Health, or a related field.
• Strong analytical, organizational, and communication skills.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
• Ability to work collaboratively in a team environment and manage time effectively.
• Passion for regulatory affairs, innovation in healthcare, and improving patient outcomes.

Learn more about our EEO & Accommodations request here.