Medical Information Manager
United Therapeutics Corporation
August 13, 2026
Remote friendly (Raleigh-Durham-Chapel Hill Area)
United States
Medical Affairs
Responsibilities:
- Collaborate with GMI Product Leads to research, develop, and maintain medical affairs materials (standard response documents, FAQs, AMCP dossiers, slide decks, leave-behinds).
- Develop and update scientifically balanced responses to unsolicited requests for on- and off-label indications; maintain and distribute a standard response database via internal review/approval.
- Assist with AMCP-format product dossiers.
- Serve as subject matter expert; stay current on emerging literature/clinical trials, translate data, and develop educational materials for internal and external HCP audiences.
- Use Veeva MedInquiry to manage medical information requests and escalations for the Contact Center Team.
- Support scientific congress booth strategies (study design handouts, adverse event management materials, pipeline overview slides); provide booth staffing; collect/report data and competitive intelligence.
- Report adverse events and product complaints to Global Patient Safety/Pharmacovigilance per SOPs and compliance requirements.
- Support maintenance of Publications Library and Clinical Trials website sections.
- Evaluate templates for Medical Information document development.
- Contribute to medical affairs workstreams, launch meetings, insights forums, and initiatives.
Minimum Requirements:
- PharmD with active pharmacy license.
- 2+ years pharmaceutical industry medical information or hospital experience.
- Experience abstracting databases (Embase, PubMed) for literature search and full-text retrieval.
- Ability to manage multiple projects to timelines/budgets.
- Awareness of Medical Information/Medical Affairs regulations/guidelines.
- Excellent organizational and verbal/written communication skills.
- Self-motivated and cross-functional collaborator.
- Proficient in Microsoft Word, PowerPoint, and Excel.
Preferred Qualifications:
- 1+ years medical writing.
- 1+ years Medical Information Fellowship.
- Experience developing field medical slides for external use.
- Membership in accredited medical writing associations (e.g., AMWA).
- Experience with IRMS or Veeva MI (end user/admin) or strong aptitude to learn systems.
- Clinical experience in pulmonary hypertension.
- Collaborate with GMI Product Leads to research, develop, and maintain medical affairs materials (standard response documents, FAQs, AMCP dossiers, slide decks, leave-behinds).
- Develop and update scientifically balanced responses to unsolicited requests for on- and off-label indications; maintain and distribute a standard response database via internal review/approval.
- Assist with AMCP-format product dossiers.
- Serve as subject matter expert; stay current on emerging literature/clinical trials, translate data, and develop educational materials for internal and external HCP audiences.
- Use Veeva MedInquiry to manage medical information requests and escalations for the Contact Center Team.
- Support scientific congress booth strategies (study design handouts, adverse event management materials, pipeline overview slides); provide booth staffing; collect/report data and competitive intelligence.
- Report adverse events and product complaints to Global Patient Safety/Pharmacovigilance per SOPs and compliance requirements.
- Support maintenance of Publications Library and Clinical Trials website sections.
- Evaluate templates for Medical Information document development.
- Contribute to medical affairs workstreams, launch meetings, insights forums, and initiatives.
Minimum Requirements:
- PharmD with active pharmacy license.
- 2+ years pharmaceutical industry medical information or hospital experience.
- Experience abstracting databases (Embase, PubMed) for literature search and full-text retrieval.
- Ability to manage multiple projects to timelines/budgets.
- Awareness of Medical Information/Medical Affairs regulations/guidelines.
- Excellent organizational and verbal/written communication skills.
- Self-motivated and cross-functional collaborator.
- Proficient in Microsoft Word, PowerPoint, and Excel.
Preferred Qualifications:
- 1+ years medical writing.
- 1+ years Medical Information Fellowship.
- Experience developing field medical slides for external use.
- Membership in accredited medical writing associations (e.g., AMWA).
- Experience with IRMS or Veeva MI (end user/admin) or strong aptitude to learn systems.
- Clinical experience in pulmonary hypertension.