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PTC Therapeutics

Biopharmaceuticals for rare genetic disorders

Medical Science Liaison - Neurology

Medical, Clinical & VeterinaryUpdated on Nov 11
Full-timeRemote in USA

About the Job

Requirements

  • An advanced scientific degree (PhD, PharmD, MD, DNP, MSN, MS, or Genetic Counselor) and at least 2 years of experience as a Medical Science Liaison are required.
  • Experience supporting an orphan product and/or prior clinical experience in neuromuscular disorders, genetics, and/or rare disease is required.
  • Experience supporting high-cost products distributed through specialty pharmacies that require extensive coordination with patient access services is required.
  • Hands-on experience working with key opinion leaders, clinicians, healthcare professionals, payors, and/or academic institutions to establish and maintain relationships and scientific or medical credibility is required.
  • Demonstrated success interpreting scientific data and presenting research information to scientists and healthcare professionals is required.
  • Verbal and written communication skills, including scientific and technical writing and presentations, and the ability to communicate complex technical information clearly are required.
  • An understanding of the pharmaceutical delivery process is required.
  • The ability to influence without direct authority is required.
  • Proficiency with Microsoft Office is required.
  • The ability to work independently and collaboratively in a fast-paced, matrixed environment with internal and external team members is required.
  • Analytical thinking, problem-solving skills, and the ability to adapt to changing priorities and deadlines are required.
  • Planning, organization, and time-management skills, including the ability to support and prioritize multiple projects, are required.
  • A valid driver’s license, personal automobile, and active vehicle insurance policy are required. The candidate must be able to travel daily to and from customer accounts and drive and/or fly long distances, depending on territory size.
  • The position requires overnight travel, with the amount varying by territory, as well as overnight and/or weekend travel outside the assigned territory.
  • Daily entry to hospitals and other medical facilities is required, and employees must meet facility vendor-credentialing requirements, including defined training, background checks, and proof of immunization.
  • The candidate should be based in the Central or West Coast time zone.

Responsibilities

  • Attend national and regional medical meetings and symposia as a company representative; engage with attendees, attend scientific sessions and poster presentations, gather and summarize findings, and cultivate professional relationships where appropriate.
  • Deliver fair-balanced, objective clinical and scientific presentations to healthcare professionals, payors, and patient organizations in response to unsolicited requests for information about company products.
  • Identify speakers for advisory boards, symposia, and educational programs, using regulatory-approved materials, slide sets, abstracts, and posters.
  • Support regional medical initiatives, including advisory boards, as needed.
  • Provide management with input regarding competitive therapies, business development opportunities and risks, and market insights.
  • Establish, manage, and maintain relationships with relevant health authorities and stakeholders, including key opinion leaders, healthcare professionals, academic institutions, payors, and patient organizations.
  • Facilitate timely and accurate submission of applications for unrestricted educational grants or research initiatives and requests for study support, in accordance with company policy.
  • Maintain awareness of medical, clinical, regulatory, compliance, and quality issues and processes applicable to company therapeutic areas, and adhere to and support company standards.
  • Maintain competitor information relevant to therapeutic areas, goals, objectives, project activities, and product-team priorities; stay current on therapeutic advances and competing therapies or products; analyze and apply intelligence findings; and efficiently communicate and present relevant data and impact to internal stakeholders.

Desired Qualifications

  • Experience supporting an orphan, rare-disease, and/or specialized drug is preferred.
  • Experience with Duchenne muscular dystrophy or Friedreich’s ataxia is preferred.

About the Company

PTC Therapeutics

Biopharmaceuticals for rare genetic disorders

PTC Therapeutics develops and commercializes treatments for rare genetic disorders worldwide, leveraging RNA biology and post-transcriptional control. Its portfolio includes Translarna (ataluren) for nonsense-mutant Duchenne muscular dystrophy, Evrysdi (risdiplam) for spinal muscular atrophy, Emflaza (deflazacort) for DMD, and Upstaza for AADC deficiency, among others. The company uses an integrated model spanning discovery, clinical development, manufacturing, and global commercialization, with operations in 50+ countries and a European base in Dublin. Its goal is to provide safe, effective therapies for patients with limited treatment options and to grow a robust pipeline in rare diseases.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Warren Township, New Jersey
Founded
1998

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