Global Medical Intern

Mallinckrodt Pharmaceuticals•Bridgewater, NJ

2d•$22,000 - $28,000•Hybrid

About The Position

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.

Requirements

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

Nice To Haves

Previous pharmaceutical industry experience is preferred but not required.

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