About The Position

The Medical Science Liaison (MSL) is a field‑based scientific expert responsible for engaging healthcare professionals, clinical experts, and key external stakeholders in support of the agreed medical strategy for Tryngolza, an innovative therapy for Familial Chylomicronemia Syndrome (FCS), with future potential in Severe Hypertriglyceridemia (sHTG). This role can be based in Nürnber, Regensburg, Munich, Augsburg, Ingolstadt, Ulm and other cities in Germany. In this role, you will drive scientific exchange, support clinical and evidence‑generation initiatives, gather actionable insights, and partner cross‑functionally to ensure consistent, high-quality scientific standards. The position plays a critical part in enhancing understanding of rare lipid disorders, supporting patient pathways, and enabling informed, ethical decision‑making. Executes field medical activities in accordance with Medical Excellence standards, including qualitative insights capture, engagement planning discipline, and agreed performance measures.

Requirements

  • Advanced life sciences degree required (e.g., PharmD, PhD, MD, MSc or equivalent).
  • Prior experience as an MSL or in a similar customer‑facing medical role preferred.
  • Experience in specialty care, metabolic disorders, or highly scientific therapy areas is strongly beneficial.
  • Proven experience engaging with HCPs, building external relationships, and driving meaningful scientific exchange.
  • Strong scientific understanding and ability to explain complex data clearly.
  • Excellent communication, presentation and interpersonal skills.
  • Ability to build credibility and trust with clinical and scientific experts.
  • Strong analytical and insight‑generation capability.
  • Comfort working autonomously in the field, with strong organizational skills.
  • Ability to collaborate effectively with internal cross‑functional teams.
  • High ethical standards and commitment to unbiased scientific engagement.
  • Flexibility to travel for external meetings, site visits, and medical events.
  • Good command of English.

Responsibilities

  • External Scientific Engagement Serve as the primary field‑based medical and scientific expert for Tryngolza within the sHTG community.
  • Build and maintain strong, trusted relationships with: Key opinion leaders (KOLs) Healthcare professionals Academic researchers
  • Conduct non‑promotional scientific discussions on disease pathways, clinical evidence, patient management, and emerging data, in line with approved medical content.
  • Ensure high‑quality, balanced scientific exchange and clear communication of relevant information.
  • Develop and maintain stakeholder engagement plans aligned to Medical Excellence guidance (segmentation, objectives, scientific exchange plans, and documentation)
  • Insight Generation & Strategic Contribution Gather and communicate actionable insights from HCP interactions, scientific meetings, and stakeholder activities.
  • Share insights with Medical Affairs colleagues to shape: Medical strategy Evidence‑generation priorities Stakeholder engagement plans Educational programs Key account plans in a cross-functional manner
  • Identify and communicate emerging gaps in diagnosis, treatment access, and unmet needs.
  • Contribute to periodic insight reviews (e.g., monthly/quarterly) to support cross-country visibility and strategic decision-making
  • Medical Education & Scientific Support Deliver scientific education to HCPs, centers, and relevant networks.
  • Support the Medical Advisor in developing educational content, disease‑awareness programs, and scientific resources.
  • Provide scientific training and support to internal teams (e.g., commercial, patient access, field teams) to ensure accuracy, consistency and compliance.
  • Support advisory boards, congress activities, and expert meetings.
  • Deliver and support education initiatives following Medical Excellence quality standards .
  • Clinical Research & Evidence Generation Contribute to evidence‑generation activities including: Phase IIIb/IV studies Investigator‑initiated research (ISS/ISR) Non‑interventional studies, registries, RWE programs Patient identification and site feasibility discussions
  • Engage with investigators and sites to support study awareness, feasibility insights, and scientific collaboration.
  • Share insights from clinical practice patterns to help inform medical and scientific strategy.
  • Compliance & Medical Governance Ensure all field activities and materials adhere to internal medical governance standards, SOPs, and external codes of practice, and follow Medical Excellence ways of working (documentation standards, tool usage, and KPI reporting expectations)
  • Deliver scientific information in a compliant, balanced, non‑promotional manner.
  • Understand and follow all medical, regulatory, and pharmacovigilance processes.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Number of Employees

501-1,000 employees

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