Integral member of the Medical Information team who leverages therapeutic and product knowledge of Novartis oncology products to optimize internal and external customer communications. This position offers an opportunity to work on cross-functional teams to support Novartis oncology products.
Create and deliver timely responses to unsolicited medical information inquiries/requests from HCPs in a multi-media environment and record information according to Novartis and regulatory guidelines
Develops and maintains response database for assigned products
Conduct medical review of promotional materials during Oncology Marketing PRT (oMAP) meetings
Collaborate with cross-functional teams to identify strategies and execute tactics to support Novartis Oncology products (e.g. medical product teams [MPT], launch management teams [LMT], Global Oncology Scientific Affairs)
Develop comprehensive compendia strategies for product by interfacing with key internal stakeholders and lead submission process
Develop and provide therapeutic and product training to multiple internal customers (e.g. sales force, customer interaction center (CIC), MSLs, clinical)
Create and update clinical section of AMCP dossier and ensure timely delivery to HCPs upon solicited requests
Perform literature review for product NDA annual submission in a timely fashion
Staff medical information booths for annual meetings in oncology, hematology, and rare diseases
Monitor, collect, and analyze metrics for MI activities and report on a regular basis
The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
BS/MS within scientific discipline required
RPh, RN, PhD, PharmD, MD; Oncology therapeutic area experience and knowledge preferred
1-2 (Mgr, Sr Mgr) or 3-5 (Assoc Dir) years of experience in medical writing, medical information/drug information, and/or relevant clinical experience
Ability to acquire knowledge of various disease states and products
Solid verbal and written communication skills
Ability to work in a matrix environment on cross-functional teams
Proven literature analysis and evaluation skills
Proficient in Microsoft Word, PowerPoint, Excel, and technologically savvy
Ability to manage multiple projects within defined timelines
Solid ability to negotiate, resolve conflicts, prioritize, and organize in a complex, matrix environment
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