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Orchard Therapeutics

Autologous gene therapies for rare diseases.

Senior Medical Science Liaison - Gene Therapy, US Medical Affairs

Biology & BiotechConfirmed live in the last 24 hours
Full-timeRemote in USA$190k - $240k

About the Job

Requirements

  • A PhD, Doctor of Pharmacy, MD, Nurse Practitioner, Doctor of Veterinary Medicine, Certified Genetic Counselor, or similar advanced scientific or healthcare degree is preferred; an RN, Master of Science, or similar qualification with substantial experience is considered.
  • At least five years of experience in a scientific, clinical, or Medical Science Liaison role within the biotechnology or pharmaceutical industry.
  • Extensive field experience as a Medical Science Liaison supporting post-approval commercial products.
  • Ability to lead and motivate team members without a direct reporting relationship, including coaching and mentoring colleagues.
  • Track record of establishing relationships with healthcare-provider thought leaders and extended clinical-care teams, becoming a preferred point of contact and trusted resource.
  • Understanding of United States government and industry guidelines, regulations, and laws for compliant exchange of scientific and clinical information with external stakeholders.
  • Experience and relevant knowledge in one or more of hematopoietic stem cell transplantation, gene therapy, and neurology/genetics; neurometabolic genetics is preferred.
  • Experience developing and delivering scientific educational materials and programs for multistakeholder and multispecialty audiences across disease states.
  • Strong knowledge of and established network with healthcare providers and industry experts.
  • Fluency in spoken and written English.
  • Valid United States driver’s license and clean driving record.
  • Ability to travel frequently (75%), often overnight.

Responsibilities

  • Identify, build, and maintain collaborative partnerships with healthcare providers, key external experts such as key opinion leaders, and academic institutions to become a trusted scientific partner.
  • Provide timely, audience-appropriate information and updates that enhance understanding of the scientific and medical value of Orchard’s programs, collaborating with Market Access, Government Affairs, Diagnostics, Patient Advocacy, Clinical Development, and other groups.
  • Maintain training records and deliver training updates so personnel in assigned Qualified Treatment Centers are appropriately trained according to Orchard’s standard operating procedures and the latest Product Manual.
  • Develop a territory profile covering Centers of Excellence, key expertise, newborn screening approaches and leaders, and market access pathways to inform medical strategy and tactical planning with Commercial, Diagnostic, and Patient Advocacy partners.
  • Gather field insights on data, the therapeutic area, and competitive intelligence to inform company strategies and evidence-generation plans.
  • Build operational understanding to ensure excellent execution and risk management within governance processes.
  • Review and oversee Investigator-Sponsored Trial requests and Early Access Program requests throughout internal review and follow-up information requests.
  • Build internal partnerships and collaborate across Medical Affairs, Patient Advocacy, Public Affairs, Clinical Development, Clinical Operations, Technical Operations, Market Access, Commercial, and other groups.
  • Ensure compliance with internal and external regulatory and legal guidelines.
  • Maintain clinical, scientific, and technical expertise in the therapeutic area.
  • Develop strategic initiatives that support departmental goals from a field medical excellence perspective.
  • Manage at least two large cross-functional projects while maintaining geographic responsibilities.
  • Proactively seek out and demonstrate successful peer coaching of other team members.
  • Develop United States field resource materials specific to stakeholder group, disease state, and technology.
  • Maintain expertise in the therapeutic area and related fields to provide strategic insights, communicate scientific insights, and support strategic objectives.
  • Monitor competitive advances and trends in the therapeutic area, including new treatment management and therapies, and provide internal stakeholders with feedback on competitor initiatives.
  • Serve as a peer leader who mentors and coaches new or junior Medical Science Liaisons, supporting onboarding, training, and field excellence.

Desired Qualifications

  • Experience and relevant knowledge in neurometabolic genetics.

About the Company

Orchard Therapeutics

Autologous gene therapies for rare diseases.

Orchard Therapeutics develops and commercializes one-time gene therapies for rare, life-threatening diseases by using a patient’s own hematopoietic stem cells (HSCs) that are collected, ex vivo edited to carry a correct gene, and reinfused to restore function. The treatment typically targets the immune and blood system, aiming to address the disease at its source with a single administration. It differentiates itself by focusing on autologous, ex vivo gene editing and a clear path to market with approved products like Libmeldy/Lenmeldy for metachromatic leukodystrophy, plus a clinical-stage portfolio for other genetic disorders. The company’s goal is to bring safe, curative therapies to patients and grow a portfolio of approved and investigational gene therapies for unmet medical needs, now under Kyowa Kirin after a 2024 acquisition.

Company size
201-500
Company stage
IPO
Headquarters
London, United Kingdom
Founded
2015

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