C
Not Specified Permanent

Dallas, Texas · USA job

Medical Science Liaison, Oncology/Hematology (Houston or Dallas Texas)

Cedent Consulting

Dallas, Texas

Job description

Overview

As an field-based medical science expert, you will foster peer-to-peer relationships with opinion leaders and translate scientific data for diverse audiences. You'll serve as a bridge between medical communities and the company, delivering clinical presentations and providing up-to-date medical information. You will support conferences, publications, investigator-initiated studies, and advisory boards, shaping medical strategies across therapeutic areas. This role offers meaningful impact by advancing scientific understanding and collaboration at a global scale.

Responsibilities
  • Deliver clinical and scientific presentations to healthcare professionals and committee members
  • Provide medical information and disease expertise to the medical community
  • Support scientific activities at medical conferences
  • Develop and maintain peer-to-peer collaborations with key medical experts
  • Respond to unsolicited medical information requests using a customized approach
  • Collaborate on medical affairs initiatives including publications and investigator-sponsored studies
  • Assist with clinical initiatives including site identification, registries, and data presentation
  • Contribute medical input to advisory boards and review speaker presentations
  • Train staff on key scientific topics and review professional slide decks and clinical summaries
  • Maintain compliance with regulatory guidelines
  • Gather clinical field insights and inform the team regularly
  • Understand the role and contributions of Medical Science Liaisons and Medical Affairs
  • Perform additional duties as assigned
Key requirements
  • Advanced scientific degree (MD, DO, PhD, PharmD) in Medical or Biological Sciences
  • Minimum of two years in Medical Affairs/Clinical functions (preferred)
  • Familiarity with drug development, FDA, ICH, and GCP guidelines
  • Experience with clinical trials in academic or industry settings (a plus)
  • Ability to review and interpret clinical data
  • Ability to develop clinical data and medical content for presentations
  • Proficient in Microsoft Office (Word, PowerPoint, Excel)
  • Strong presentation skills
  • Project management experience (a plus)
  • Experience with rare diseases (a plus)
  • Independent work capability and strong time management
  • Excellent written and verbal communication skills
  • Strong relationship-building
  • Clear and persuasive communication
  • Self-motivated and ethical conduct
  • Clinical data interpretation
  • Medical content development
  • Presentation design and review

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