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14 часов назад

Project Manager

Формат работы
onsite
Тип работы
fulltime
Грейд
junior/middle
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

Project Manager (Medtech): Leading broadcast projects through the Medical/Legal/Regulatory (MLR) process from sale to launch with an accent on content submission, quality control, and timeline management. Focus on coordinating cross-functional teams and ensuring digital assets meet strict regulatory standards in a fast-paced environment.

Location: Must be based in Yardley, Pennsylvania, United States

Company

hirify.global is a leading provider of health information services, connecting medical professionals and patients through digital platforms and live events.

What you will do

  • Manage end-to-end project lifecycles from initial sale to final launch.
  • Prepare and edit documentation for pharmaceutical regulatory submission processes.
  • Perform thorough editorial and quality control checks on all project materials.
  • Coordinate execution across Account, Creative, Technology, and Event teams.
  • Monitor project timelines and provide regular status updates using project management software.
  • Interpret and address regulatory feedback to ensure compliance of websites, videos, and digital assets.

Requirements

  • Must be based in or able to work from Yardley, Pennsylvania.
  • Minimum 1-2 years of experience in pharmaceutical advertising or a similar fast-paced environment.
  • Proficiency in Microsoft Office suite (Word, Excel, Outlook).
  • Strong organizational and analytical skills with high attention to detail.
  • Ability to multitask and meet strict deadlines in a high-pressure setting.
  • Excellent verbal and written communication skills.

Nice to have

  • Knowledge of Adobe InDesign.
  • Experience with project management software tools.

Culture & Benefits

  • Opportunity to work in a major healthcare information organization.
  • Collaborative environment working with diverse internal teams.
  • Exposure to pharmaceutical regulatory processes and digital media production.

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