Hybrid Clinical Trials Intern - Admin & Project Support

Worldwide; North Carolina; Hybrid; USD 32,000 - 64,000; Part time

Benefits offered by this job

Competitive benefits package

Job summary

Worldwide Clinical Trials, a global midsize CRO, is seeking a Clinical Trials Associates Intern for a hybrid US-based role in North Carolina. This internship emphasizes hands-on administrative and project training support within the clinical project team.

Responsibilities include managing system access, document control, and shipment of trial materials, with final evaluation of learning outcomes across projects. Applicants must be university students in Clinical Research programs.

Qualifications

• Enrolled in Clinical Research program or master’s level program at an accredited university.
• Not required to have prior experience.
• Not required certifications.

Responsibilities

• Arrange and track system access for project team (PMs, Lead CRAs, CRAs).
• Maintain quality audit checks for current document revisions on project portals.
• Assist with preparation and shipment of clinical trial documentation (Investigator Site File).
• Maintain version control of project documentation and submit to trial master file.
• Track and maintain project-related information, including site medical questions and answer logs.

Skills

Microsoft Office Suite

Written and oral communication

Presentation skills

Attention to detail

Organizational skills

Problem-solving

Analytical skills

Prioritization

Interpersonal skills

Education

University student enrolled in Clinical Research Program or Master’s program

Job description

Worldwide Clinical Trials, a global midsize CRO, is seeking a Clinical Trials Associates Intern for a hybrid US-based role in North Carolina. This internship emphasizes hands-on administrative and project training support within the clinical project team.

Responsibilities include managing system access, document control, and shipment of trial materials, with final evaluation of learning outcomes across projects. Applicants must be university students in Clinical Research programs.