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14 часов Π½Π°Π·Π°Π΄

Sr. Manager, Patient Advocacy, Global Rare Diseases

128Β 070 - 156Β 530$
Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
hybrid
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
senior
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
US
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

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TL;DR
Sr. Manager, Patient Advocacy, Global Rare Diseases (Rare Disease Patient Advocacy): Developing and executing patient advocacy programs for hereditary angioedema across the Americas with an accent on partnerships with patient advocacy organizations, patient education, and cross-functional collaboration. Focus on representing the patient voice in internal decision-making, building compliant stakeholder relationships, and implementing advisory boards, speaker engagement, and policy advocacy initiatives.

Location: Based in Boston, Massachusetts; hybrid work arrangement with approximately 40% national and international travel

Annual base pay: $128,070–$156,530

Company

hirify.global is an international research-focused biopharmaceutical group developing and commercializing medicines and patient support services, including treatments for rare and ultra-rare disorders.

What you will do

  • Contribute to the global rare disease patient advocacy strategy and execute programs across the Americas.
  • Develop plans to engage patient communities in the United States and Canada while coordinating with the LATAM patient advocacy team.
  • Build and maintain long-term partnerships with patient advocacy organizations and other stakeholders.
  • Design and implement educational programs, advisory boards, patient speaker engagements, policy advocacy initiatives, and related partnerships.
  • Represent the patient perspective in strategy meetings and educate cross-functional teams on patient needs and insights.
  • Conduct stakeholder engagements in accordance with legal, compliance, and regulatory requirements.

Requirements

  • 5+ years of experience in a biopharmaceutical environment, including at least 2 years in rare disease and patient advocacy.
  • Bachelor’s degree in social science, public health, science, or a related field.
  • Strong communication, networking, listening, interpersonal, project management, and program management skills.
  • Ability to build trust with diverse stakeholders and collaborate across internal functions and external organizations.
  • Understanding of drug research and development, regulatory requirements, compliance, and disclosure guidelines.
  • Must be based in Boston and able to travel nationally and internationally approximately 40% of the time.

Nice to have

  • Advanced degree.

Culture & Benefits

  • Development opportunities with access to training and professional resources.
  • Comprehensive healthcare programs and work-life balance initiatives.
  • Relocation support and tax assistance services for foreign colleagues.
  • Flexible working arrangements and remote work options within the role’s location framework.
  • Performance bonuses and market-benchmarked benefits.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’