Global Medical Intern

Job Title

Global Medical Intern

Requisition

JR000015673 Global Medical Intern (Open)

Location

Bridgewater, NJ

Additional Locations

Job Description Summary

Job Description

The Global Medical Information (GMI) Intern provides clinical and scientific support for Keenova Therapeutics’ products. This role offers hands-on experience within Medical Affairs and exposure to cross-functional collaboration in a global pharmaceutical environment.

 

Key Responsibilities:

• Comply with all relevant guidelines, standards, and regulations pertaining to unsolicited medical information inquiries in liaison with the preceptor and in accordance with Keenova Therapeutics’ Standard Operating Procedures (SOPs).

• Manage unsolicited medical information requests, under supervision, escalated from the Global Medical Information (GMI) Call Center or received directly from healthcare professionals (HCPs), payers, patients, and caregivers, including complex and off-label inquiries.

• Draft accurate, fair-balanced, and scientifically sound responses to medical inquiries under the guidance and review of the preceptor and in compliance with company requirements.

• Critically evaluate medical and scientific literature, with oversight, to develop evidence-based response documents and ensure timely completion of Medical Information Request Forms (MIRFs).

• Assist in the creation and review of medical content for both promotional and non-promotional materials, ensuring scientific accuracy, appropriate referencing, and fair balance under committee supervision.

• Attend interdisciplinary Medical Affairs meetings, gaining exposure to cross-functional collaboration.

• Support insight generation and preparation of analytical reports on pharmaceutical products, as applicable.

• Generate product insights and prepare analytical reports on pharmaceutical products, as applicable.

• Conducts a final presentation on the internship experience to the broader Research and Development Department.

• Deliver a final presentation summarizing internship experience, learnings, and contributions to the broader Research and Development Department.

Minimum Requirements:

• Deliver a final presentation summarizing internship experience, learnings, and contributions to the broader Research and Development Department.

  • Preference given to candidates in the professional years of a pharmacy program.

• Previous pharmaceutical industry experience is preferred but not required.

• Basic understanding of pharmaceutical products, disease states, and Medical Information functions, with a demonstrated willingness to learn clinical data and internal process management.

• Foundational scientific knowledge with the ability to effectively research medical databases and gather relevant literature to support inquiries, projects, or response documents.

• Strong written communication skills are preferred, with the ability to draft and review scientific materials clearly and accurately.

• Demonstrated diligence, professionalism, integrity, and a genuine desire to learn and grow in a Medical Affairs environment.

• Proficiency in Microsoft Office applications (Word, Excel, PowerPoint, SharePoint Outlook) with willingness to further develop technical competencies.

 

Relationship with Others/Scope of Position:

This role will report to the “Associate Director, Medical Review”.  This intern will collaborate and interact with multiple cross-functional departments including but not limited to: Research & Development, Medical Affairs, Legal, Regulatory, Quality, Product Monitoring, Pharmacovigilance, Manufacturing, Customer Service, and Commercial.

Working Conditions: hybrid role; 3 days/week onsite

The expected base pay range for this position is $22K - $28K. The offered rate of pay will vary according to the candidate's current degree program and level of study.

Disclaimer:  The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications.  Management reserves the right to change or modify such duties as required.

#LI-GN1 and #LI-HYBRID

At Keenova, we believe that no one should be alone in their pursuit of better health. This purpose drives us as we pair quality therapeutics with human support—showing up in big moments and small to help patients find comfort and confidence.

 

We bring deep expertise and resolve to every therapeutic area we serve, including immunology, urology, men’s health, orthopedics, critical care, and pediatric endocrinology. We work with patients, care partners, and physicians to help them navigate healthcare system complexity and access therapies that make a meaningful difference.

 

We are Keenova—keen to solve, keen to serve. Learn more at www.keenova.com.