project managementbusiness developmentcrocmcmandarincmopharmaceuticalsdrug development
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Мало
$105к-120к/год
$120к$150кмедиана$170к
По похожим ролям (48) ~ $150к/год
На СНГ рынке: $3.2к/мес ($2.2к - $4.7к)
70
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Зона ответственности в фармацевтической разработке описана понятно, но для уровня Senior Manager/Associate Director указан всего лишь предпочтительный опыт от двух лет.
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Ниже рынкаПонятная зона ответственностиНесоответствие уровняФокус на фарме
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Manager/Associate Director, CMC Project Management (Pharmaceuticals): Managing drug substance and drug product projects from proposal through completion with an accent on project planning, client communication, technical coordination, and business development. Focus on controlling timelines and budgets, resolving project issues, and coordinating cross-functional teams in the pharmaceutical development environment.
Location: Remote, United States; candidates must be in the Eastern time zone.
Annual base salary: $105,000–$120,000.
Company
hirify.global's STA Pharmaceutical business provides pharmaceutical development and manufacturing services.
What you will do
Manage drug substance and drug product projects from proposal preparation through completion.
Support business development by preparing quotations and proposals with key stakeholders.
Plan projects, define objectives, timelines, deliverables, tasks, and resource requirements.
Monitor project progress, schedules, budgets, risks, and corrective actions, and report updates to stakeholders.
Act as the liaison with clients, lead project meetings, prepare agendas and minutes, and track action items.
Support customer visits, conferences, and trade shows while evaluating project results and recommending improvements.
Requirements
Master's degree or PhD in Chemistry or Pharmaceutical Sciences.
Bilingual fluency in English and Mandarin.
Strong project management, problem-solving, interpersonal, verbal, written, and presentation skills.
Proven ability to work cross-functionally across technical, business, and operational areas.
Good understanding of the pharmaceutical industry and small-molecule drug development.
Proven experience creating and carrying out successful plans and processes.
Self-starter with strong organization, attention to detail, motivation, and flexibility.
Ability to use Microsoft Office products.
Nice to have
2 or more years of pharmaceutical or CRO/CMO industry experience.
Project management experience.
Experience in a Contract Research Organization or Contract Manufacturing Organization.
Culture & Benefits
Remote work arrangement for candidates in the Eastern time zone.
Cross-functional collaboration with business units, technical teams, project management, clients, and business development.
Participation in customer visits, conferences, and trade shows.
Equal opportunity employment.
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