Medical Science Liaison - Neuromuscular & Duchenne (Hybrid)

Sarepta Therapeutics

Illinois

Hybrid

USD 173,000 - 217,000

Full time

14 days+

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Job summary

Sarepta Therapeutics is seeking a Medical Science Liaison (MSL) to build peer-to-peer relationships with healthcare professionals in neuromuscular diseases, focusing on Sarepta’s marketed and investigational products. The MSL will serve as a scientific resource, communicating complex data in a compliant, non-promotional manner.

The candidate should have a graduate-level degree (MD/PhD/PharmD) and at least 3 years of relevant experience, with extensive travel (>50%) and a hybrid work arrangement

Qualifications

  • Graduate level degree (MD, PhD, PharmD) or equivalent required.
  • Minimum of 3 years of work experience in research and development, clinical trials, medical information, clinical practice, or other related position(s) pertinent to our therapeutic areas; Medical Affairs / MSL experience preferred.
  • Demonstrates strong emotional intelligence, optimism, and a solutions-oriented mindset
  • Proven ability to effectively communicate advanced concepts to stakeholders
  • Familiarity with and track record of complying with industry and regulatory compliance guidelines
  • Demonstrated ability to work independently and in collaborative team environment
  • Willingness to travel >50% of time
  • Experience and expertise in clinical trial design / execution and interpretation of scientific data
  • High integrity, sense of urgency, ability to recognize time sensitivity
  • Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills

Responsibilities

  • Identifies, establishes, and fosters peer-to-peer relationships with Key Opinion Leaders (KOLs), clinicians and researchers within disease state areas aligned to Sarepta's marketed and investigational products, e.g. neuromuscular experts
  • Develops and implements rolling and goal-oriented KOL field engagement strategy that demonstrates ownership of the execution of the medical strategy, projects and initiatives with their region
  • Demonstrates strong knowledge of disease-state and product/platform data through communication of complex clinical data and product information in a clear, compliant, and non-promotional manner
  • Collects high quality, actionable feedback and reports trends and unmet medical needs, leading to strategic impact
  • Deliver high-quality presentations of scientific data to health care professionals in various settings, including peer-to-peer meetings, advisory boards, investigator meetings, and other appropriate venues to enhance product / disease state knowledge
  • Supports investigator-initiated studies (IIS/SRA), regional research collaborations, registries, and other evidence generation activities.
  • Assesses site capabilities with regard to the effective conduct of these various forms of clinical research, providing feedback to internal teams.
  • Provide professional medical affairs representation and support at global, national and regional scientific meetings, including but not limited to staffing medical affairs booths, gathering competitive intelligence, and partnering to develop post-conference scientific materials
  • Develop and maintain clinical expertise in Duchenne muscular dystrophy through review of scientific journals, recent data disclosures and participation in scientific congresses
  • Maintain strong working relationships with cross-functional field, GMA peers, and other internal teams to provide a compliant, coordinated approach to engagement and effective project management and execution
  • Completes all MSL administrative tasks (Veeva, Concur, compliance wire etc.), initiatives, and projects on time

Job description

Sarepta Therapeutics is seeking a Medical Science Liaison (MSL) to build peer-to-peer relationships with healthcare professionals in neuromuscular diseases, focusing on Sarepta’s marketed and investigational products. The MSL will serve as a scientific resource, communicating complex data in a compliant, non-promotional manner.

The candidate should have a graduate-level degree (MD/PhD/PharmD) and at least 3 years of relevant experience, with extensive travel (>50%) and a hybrid work arrangement

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