Medical Information Manager

California, US residents click here.

The job details are as follows:

Who We Are

We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.

United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter’s pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF).

The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.

Who You Are

You are someone who likes to triage questions.  You can research, review and synthesize information, crafting appropriate and informative responses whether my email or phone.  You love to collaborate with teammates and share your knowledge and are excited to be part of an innovate company that is passionate and inspiring.

The primary objectives of this role are to develop and maintain medical affairs materials that support all stages of a brand's life cycle, including standard response documents, frequently asked questions, and educational resources such as slide decks and leave behinds. This role is responsible for communicating in writing or verbally, relevant scientific medical information that is consistent, current, accurate, and fair-balanced in a timely manner to healthcare providers that use United Therapeutics products. The MIM will be adept at recognizing and capturing adverse events and product complaints and escalate to Global Patient Safety. They will be an expert in Veeva MedInquiry electronic system and assure consistency in documentation of cases to produce meaningful metrics.

• 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, educational resources such as slide decks and leave behinds.
• Develop and update scientifically balanced responses to unsolicited request for both on- and off-label indications. Assist in maintaining a standard response database by obtaining internal review and approval; Maintain and distribute as appropriate and necessary
• Assist in the development and maintenance of AMCP format product dossiers
• Act as a subject matter data on UT products and data. Stay abreast of emerging scientific literature and clinical trial data, translate the 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 to 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 reporting data and competitive intelligence and other insights
• Report adverse events and product complaints in a timely manner to Global Patient Safety/Pharmacovigilance according to SOPs and Compliance
• Assist in maintaining the Publications Library and Clinical Trials sections of our Corporate website
• Evaluate existing templates used in writing Medical Information documents
• Contribute actively to medical affairs workstreams, launch meetings, insights forums and other projects/initiatives