Назад
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5 дней назад

Senior Project Manager

152 000 - 190 000$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Project Manager (Clinical Drug Development): Leading cross-functional planning and execution of clinical drug development programs from study start-up through execution with an accent on clinical timelines, vendor oversight, risk management, and cross-functional coordination. Focus on integrating complex workstreams, tracking critical-path activities, and resolving delays or resource gaps across Clinical Operations, Regulatory, Safety, Biostatistics, Data Management, CMC, and DMPK.

Location: Hybrid at the San Diego headquarters; on-site work is required

Salary: $152K–$190K annually

Company

hirify.global Therapeutics is a clinical-stage life-science and technology company developing medicines through an AI-driven discovery and development platform.

What you will do

  • Lead planning, execution, and tracking of clinical drug development timelines and deliverables.
  • Develop and maintain integrated project plans covering scenario planning, resource forecasting, risks, and budgets.
  • Partner with Clinical Operations to manage study timelines and critical-path activities from start-up through execution.
  • Oversee third-party vendor relationships, including CRO scope, deliverables, timelines, and performance.
  • Facilitate cross-functional meetings, document decisions, track action items, and maintain project records.
  • Identify risks, delays, and resource gaps, and lead mitigation planning across clinical development functions.

Requirements

  • Bachelor’s degree in science, healthcare, or business with 7+ years of project management experience in the pharmaceutical or biotechnology industry, or a master’s degree with 5+ years of experience.
  • Experience managing timelines, cross-functional coordination, and third-party vendor relationships.
  • Familiarity with regulatory submission processes and Clinical Operations.
  • Excellent organizational, communication, and interpersonal skills.
  • Proficiency with project management tools such as Smartsheet, SharePoint, Confluence, or similar.

Nice to have

  • Experience in oncology drug development.
  • PMP certification or formal project management training.

Culture & Benefits

  • Inclusive environment built around diverse backgrounds, cultures, and life experiences.
  • Company-paid healthcare and flexible spending accounts.
  • Voluntary life insurance and 401(k) matching.
  • Uncapped vacation.
  • State-of-the-art San Diego facility with an on-site gym and dining.

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