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PTC Therapeutics

Biopharmaceuticals for rare genetic disorders

Medical Science Liaison - Metabolic

Biology & BiotechUpdated on Nov 11
Full-time

About the Job

Requirements

  • An advanced scientific degree (PhD, PharmD, MD, DNP, MSN, or MS), or qualification as a Registered Dietician or Genetic Counselor, and at least two years of experience as a Medical Science Liaison.
  • Experience supporting an orphan product and/or prior clinical experience in Inborn Errors of Metabolism, genetics, and/or rare diseases.
  • Experience supporting high-cost products distributed through a specialty pharmacy and requiring extensive coordination with patient access services.
  • Hands-on experience working with KOLs, clinicians, HCPs, payors, and/or academic institutions to establish and maintain relationships and scientific or medical credibility.
  • Demonstrated success interpreting scientific data and presenting research information to scientists and HCPs.
  • Verbal and written communication skills, including scientific and technical writing and presentations, and the ability to communicate complex technical information clearly.
  • Understanding of the pharmaceutical delivery process.
  • Ability to influence without direct authority.
  • Proficiency with Microsoft Office.
  • Ability to work independently and collaboratively in a fast-paced, matrixed environment with internal and external team members.
  • Analytical and problem-solving skills, adaptability to changing priorities and deadlines, and planning, organization, and time-management skills, including the ability to support and prioritize multiple projects.
  • A valid driver’s license, personal automobile, and active vehicle insurance policy; ability to travel daily to customer accounts and drive and/or fly long distances.
  • Ability to undertake overnight travel, including overnight and/or weekend travel outside the assigned territory.
  • Ability to meet facility vendor credentialing requirements, including required training, background checks, and proof of immunization, for entry to hospitals and other medical facilities.

Responsibilities

  • Attend national and regional medical meetings and symposia as a company representative; engage with attendees, attend scientific sessions and poster presentations, gather information, 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 on competitive therapies, business development opportunities and risks, and market insights.
  • Establish, manage, and maintain relationships with relevant health authorities and stakeholders, including KOLs, HCPs, 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 relevant to PTC therapeutic areas, and adhere to and support company standards.
  • Maintain competitor information relevant to company 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 communicate and present relevant impact to appropriate internal stakeholders.

Desired Qualifications

  • Experience supporting an orphan, rare-disease, and/or specialized drug.
  • Experience in Phenylketonuria 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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