✨ About The Role
- The Intern/Advanced Intern will assist in researching, writing, and editing regulatory documents such as clinical study protocols and reports.
- The role involves quality control project management activities to ensure the accuracy of medical writing deliverables.
- Interns will participate in professional development opportunities and training throughout the program.
- The internship requires a commitment to work onsite in RTP, NC, for the duration of the program from May through August 2025.
- Interns will have the opportunity to make a meaningful impact in a patient-centric environment.
âš¡ Requirements
- The ideal candidate is a college student actively pursuing a degree in biological science or a related field.
- Strong writing and editing skills are essential for creating regulatory documents and ensuring quality control.
- Proficiency in Microsoft Office is required to assist in various documentation tasks.
- The candidate should be detail-oriented and capable of following standard operating procedures and style guides.
- A proactive attitude towards learning and professional development will be beneficial in this role.