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Intern University Program - Clinical Operations

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

Intern University Program – Clinical Operations

πŸ“ Location: Daytona Beach, FL (On-Site)
πŸ“‚ Category: Clinical
πŸ†” Job ID: 255160
πŸ’Ό Type: Internship (Early Careers Program)


🌟 About the Program

At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers Program is more than just an internship — it’s a launchpad for your future.

As an Intern, you’ll become part of a global clinical research team where curiosity, learning, and collaboration are encouraged. Through hands-on projects, mentorship, and structured training, you’ll gain real-world experience in clinical operations, research, and data-driven healthcare innovation.

We don’t expect you to know it all — what matters most is your potential, motivation to learn, and willingness to grow.

πŸš€ Your journey to pioneering tomorrow’s breakthroughs starts here.


🧭 Job Overview

The Clinical Research Intern will support one of the following departments:

  • Clinical Operations

  • Statistical Programming

  • Data Management

  • Drug Safety

  • Project Management

You’ll assist in the planning, execution, and oversight of clinical trials, gaining exposure to both operational and analytical aspects of research. This program is designed for students or recent graduates eager to build a career in clinical development, trial management, or data-driven research.

πŸ“ Work Arrangement: On-Site (Daytona Beach, FL)


🧩 Key Responsibilities

πŸ“„ Documentation & Compliance

  • Assist in the preparation, review, and maintenance of essential clinical trial documents (protocols, ICFs, CRFs).

  • Support preparation of materials for regulatory submissions ensuring compliance with GCP and applicable guidelines.

  • Help maintain inspection readiness and assist in internal audits.

πŸ“Š Operational Support

  • Support clinical site communication and coordination.

  • Track enrollment progress, visit schedules, and overall study status.

  • Perform data entry, tracking, and quality control tasks.

  • Assist with administrative and documentation duties for assigned projects.

πŸ’» Data & Technology

  • Support statistical programming tasks (data cleaning, validation, report generation).

  • Assist in testing and development of data management tools and electronic data capture (EDC) systems.

  • Conduct literature reviews and summarize key findings for ongoing studies.

🧠 Learning & Collaboration

  • Work closely with cross-functional teams and receive mentorship from experienced professionals.

  • Contribute ideas and participate in team discussions for process improvements.

  • Perform additional tasks as needed to ensure the department’s success.


πŸŽ“ Qualifications (Minimum Required)

  • Currently enrolled in or recently graduated from a Bachelor’s or Master’s program in:

    • Life Sciences

    • Public Health

    • Statistics

    • Computer Science

    • Pharmacy

    • Or a related field

  • Demonstrated interest in clinical research, operations, data management, or programming

  • Strong organizational and time management skills

  • High attention to detail and commitment to quality

  • Effective communication and team collaboration skills

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)

  • Ability to handle confidential information responsibly


πŸ’‘ Preferred Skills

  • Familiarity with Good Clinical Practice (GCP) and clinical trial processes

  • Experience using:

    • CTMS (Clinical Trial Management Systems)

    • EDC platforms

    • Statistical tools (e.g., SAS, R)


🧭 Work Environment

  • Office-based environment with exposure to standard electrical office equipment

  • Occasional travel (domestic/international) may be required


πŸ’ͺ Physical Requirements

  • Frequently stationary (6–8 hours/day)

  • Regular hand movements for computer use

  • Occasional crouching, stooping, bending, or twisting

  • Light to moderate lifting (up to 15–20 lbs)

  • Consistent attendance and flexibility for varied work hours


🀝 Why Join Fortrea’s Internship Program?

βœ… Gain hands-on experience in real clinical projects
βœ… Learn from industry experts and global teams
βœ… Build a foundation for a career in Clinical Research, CDM, PV, or Biostatistics
βœ… Develop professional confidence, technical skills, and industry awareness


πŸ”— Learn more: [EEO & Accommodations Request Information] (Insert official link if available)