Medical Information Manager

United Therapeutics•Rtp, NC

18h•Hybrid

About The Position

United Therapeutics (Nasdaq: UTHR) is seeking a Medical Information Manager to develop and maintain medical affairs materials that support all stages of a brand's life cycle. This role is responsible for communicating relevant scientific medical information to healthcare providers in a timely, accurate, and fair-balanced manner. The Medical Information Manager will also be responsible for capturing and escalating adverse events and product complaints, and will be an expert in Veeva MedInquiry to ensure consistency in documentation and produce meaningful metrics. The company is a public benefit corporation focused on developing novel pharmaceutical therapies and technologies to address rare, deadly diseases and the shortage of transplantable organs.

Requirements

Doctor of Pharmacy (PharmD) with an active pharmacy license
2+ years of pharmaceutical industry medical information experience or hospital experience
Experience in abstracting database (Embase and PubMed) for literature searches and full-text document retrieval
Ability to manage multiple projects simultaneously and according to agreed upon time lines and budgets
Awareness of regulations and guidelines related to Medical Information and Medical Affairs
Excellent organizational skills
Superb verbal and written communication skills
Self-motivated with a willingness to learn new skills
Demonstrated ability to work cross-functionally and be an exceptional collaborator
Proficient in Microsoft Word, Power Point, and Excel with database experience

Nice To Haves

1+ years of medical writing experience
1+ years of a Medical Information Fellowship
Experience and knowledge with developing field medical slides for external use
Participation in accredited medical writing associations (e.g. American Medical Writers Association)
Experience with Information Request Management Systems (IRMS) or Veeva MI as an end user and/or administrator, or demonstrated technical aptitude with the ability to quickly learn new systems and processes
Clinical experience in pulmonary hypertension

Responsibilities

Collaborate with GMI Product Leads to research, develop, and maintain materials supporting all stages of a brand’s life cycle, including standard response documents, frequently asked questions, AMCP dossiers, and educational resources such as slide decks and leave behinds
Develop and update scientifically balanced responses to unsolicited requests for both on- and off-label indications; assist in maintaining a standard response database by obtaining internal review and approval and maintaining and distributing responses, as appropriate
Assist in the development and maintenance of AMCP-format product dossiers
Act as a subject matter expert on company products and data; stay abreast of emerging scientific literature and clinical trial data, translate data into applicable knowledge, and develop educational materials for key internal and external HCP audiences
Develop a working knowledge of Veeva Med Inquiry to efficiently manage medical information requests and escalations supporting the Contact Center Team and ensure timely, accurate responses
Assist in the planning and execution of scientific congress booth strategies, including the creation of study design handouts, adverse event management materials, and pipeline overview slides; provide staffing support for Medical Information and Medical Affairs booths; collect and report data, competitive intelligence, and other insights
Report adverse events and product complaints to Global Patient Safety/Pharmacovigilance in a timely manner in accordance to SOPs and compliance requirements
Assist in maintaining the Publications Library and Clinical Trials sections of the corporate website
Evaluate existing templates used in the development of Medical Information documents
Actively contribute to medical affairs workstreams, launch meetings, insights forums, and other projects and initiatives