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Kiniksa Pharmaceuticals

Biopharmaceutical therapies for debilitating diseases

Medical Science Liaison

Clinical Research OperationsConfirmed live in the last 24 hours
Full-time$210k - $250k

About the Job

Requirements

  • An MD, PharmD, PhD, DO, NP, PA, MS-CGC, or other advanced scientific degree, plus at least 3 years of relevant industry, field medical, or clinical experience, is required; 1–3+ years of MSL experience is preferred.
  • Ability to communicate scientific and medical information effectively to diverse audiences and make presentations.
  • Ability to build and maintain relationships with thought leaders, subject matter experts, and other healthcare professionals.
  • Experience collaborating with internal and external stakeholders.
  • Commitment to compliance and ethical standards.
  • Ability to multitask and change course quickly.
  • Ability to travel up to 75% of the time, primarily within the assigned territory, including weekends and overnight stays as needed.

Responsibilities

  • Develop and execute a territory strategic and tactical plan aligned with Kiniksa’s medical and scientific needs.
  • Identify, cultivate, and maintain relationships with key thought leaders and stakeholders nationally and regionally to increase scientific and clinical knowledge of products, maximize MSL team impact, and drive disease awareness and, if applicable, product acceptance.
  • Support commercial and headquarters integration with targeted thought leaders by facilitating collaboration aligned with Kiniksa’s mission, strategy, and objectives through one-on-one interactions, small-group discussions, and presentations.
  • Drive ongoing clinical trial execution at study sites in collaboration with Clinical Research and Development, Clinical Operations, Regulatory Affairs, and Program Management, including site identification, evaluation and training, recruitment, and participation at investigators’ meetings.
  • Document and communicate field medical insights to internal stakeholders continuously.
  • Establish a role as a reliable and trusted resource for accurate, up-to-date medical and scientific knowledge.
  • Build and maintain technical and clinical expertise across therapeutic areas to enable in-depth scientific discussion externally, coordinating and collaborating continuously with Kiniksa’s research and development team.
  • Serve as a primary scientific resource for staffing at scientific congresses, discussions at advisory boards, and training internal colleagues.
  • Partner cross-functionally with Kiniksa team members to optimize product strategy alignment, provide medical input to interdepartmental projects, and provide clinical education to internal teams when necessary.
  • Plan and attend selected national and regional scientific meetings in cardiology and rheumatology, and prepare summaries of key findings.
  • Respond accurately, using internally approved information, and in a timely manner to unsolicited field requests for medical information from healthcare professionals.
  • Comply with applicable internal and external guidelines, policies, and procedures.
  • Maintain annual expenses within assigned budget parameters.
  • Document field activities accurately and in a timely manner.

Desired Qualifications

  • Clinical or therapeutic experience in cardiology, rheumatology, or immunology.
  • Experience with biologic immunotherapies.
  • Experience in rare diseases and orphan drug launches.
  • MSL experience, preferably 1–3+ years.

About the Company

Kiniksa Pharmaceuticals

Biopharmaceutical therapies for debilitating diseases

Kiniksa Pharmaceuticals develops and delivers therapies for patients with serious diseases that have few good treatment options. The company focuses on research and development, conducts clinical trials, and then brings approved therapies to market. Its products are created through an R&D process and are intended to be used by patients via the healthcare system, with outcomes measured to help save or improve lives. What sets Kiniksa apart is its patient-centric approach and commitment to urgency and integrity, along with a business model that combines internal R&D with partnerships and licensing to bring therapies to patients. The company aims to improve patient outcomes and quality of life by delivering effective treatments where options are limited.

Company size
201-500
Company stage
IPO
Headquarters
Lexington, KY
Founded
2015

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