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Senior medical science liaison/medical science liaison – southwest region

Valladolid
Scorpion Therapeutics
Publicada el Publicado hace 21 hr horas
Descripción

Role Summary

Senior Medical Science Liaison (MSL) for Beam Therapeutics’ Southwest Region. Owns a defined US territory with primary responsibility in sickle cell disease (SCD) and shared accountability across the Beam pipeline, including Alpha-1 antitrypsin deficiency (Alpha-1) and glycogen storage disease 1a (GSD). Architect territory strategy, onboard priority treatment centers, engage KOLs and healthcare professionals, generate actionable insights, and drive pre-commercial launch readiness in close collaboration with cross‑functional partners.

Responsibilities
* Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups; prioritize accounts and set measurable objectives.
* Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements; partner with internal teams for qualification and activation.
* Build trusted relationships with KOLs and HCPs: deliver fair‑balanced, evidence‑based education on rare diseases, cell and gene therapy science, and Beam’s platform; foster advocacy and awareness.
* Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space.
* Generate high‑quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross‑functional partners.
* Collaborate on pre‑launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch.
* Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence.
* Partner cross‑functionally with Commercial, Market Access, and Clinical teams while preserving medical independence; coordinate account plans to ensure seamless patient access and avoid duplication.
* Represent the company at congresses and external scientific meetings: plan and execute presence, engage in meaningful scientific exchanges, and follow up to strengthen visibility and credibility.
* Provide education and resources to treatment centers on operational readiness for advanced therapies, including apheresis and cell‑handling processes.
* Serve as a trusted resource for compliance and ethical standards: ensure all interactions and materials meet company policies, regulatory requirements, and industry codes.
* Maintain operational excellence: document activities and insights in CRM, monitor KPIs, and continuously improve processes, content, and tools.
* Prepare and deliver training for internal teams and external stakeholders on rare disease management and CGT fundamentals to support launch readiness.
* Act as a scientific ambassador for the company: articulate the value of the platform and pipeline to diverse audiences including clinicians, researchers, and advocacy groups.
* Monitor evolving evidence and competitive landscape in rare disease and CGT; share updates internally to inform strategy and decision‑making.
Qualifications
* Advanced scientific degree (PharmD, PhD, MD, or equivalent).
* ~10+ years industry experience in Medical Affairs with significant Field Medical tenure.
* Rare disease expertise required; hematology strongly preferred with emphasis on SCD.
* Small biotech experience preferred; demonstrated impact in resource‑constrained settings.
* Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments.
* Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy).
* Independent, proactive operator with strong ownership;
* Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity.
* Outstanding communication skills; ability to translate complex science into clear, credible narratives.
* Analytical strength for insight collection, synthesis, and actionable recommendations.
* Travel up to ~60% across assigned territory.
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