Medical Information Manager

Scorpion Therapeutics; Chapel Hill (NC); On-site; USD 100,000 - 140,000; Full time

Job summary

Scorpion Therapeutics is seeking a PharmD with an active license to join the Medical Information team. You will research, develop, and maintain medical affairs materials, respond to unsolicited requests, and support AMCP dossiers.

You will stay current on literature and clinical trials, translate data for internal and external HCP audiences, and use Veeva MedInquiry to manage information requests. Strong collaboration across functions is essential.

Qualifications

• PharmD with active pharmacy license.
• 2+ years in pharmaceutical medical information or hospital setting.
• Experience abstracting Embase/PubMed for literature search.
• Ability to manage multiple projects to timelines/budgets.
• Awareness of Medical Information regulations/guidelines.
• Excellent organizational and verbal/written communication skills.
• Proficiency in Word, PowerPoint, and Excel.

Responsibilities

• Collaborate with product leads to research, develop, and maintain medical affairs materials (FAQs, dossiers, slide decks).
• Develop and update scientifically balanced responses to unsolicited requests; maintain a standard response database.
• Assist with AMCP-format product dossiers.
• Serve as subject matter expert; stay current on literature and clinical trials; translate data for HCP audiences.
• Use Veeva MedInquiry to manage medical information requests and escalations for the Contact Center Team.
• Support scientific congress booth strategies and staff booths; report data and competitive intelligence.
• Report adverse events and product complaints to Global Patient Safety per SOPs.
• Maintain Publications Library and Clinical Trials website sections.
• Evaluate templates for MI document development.
• Contribute to medical affairs workstreams and launch initiatives.

Skills

Literature search and review

Project management

Regulatory compliance knowledge

Communication skills

Cross-functional collaboration

Self-motivated

Education

PharmD

Active pharmacy license

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Job description

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.