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3 дня назад

Associate Clinical Trial Management Director (ACTMD)

106 100 - 295 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
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
Associate Clinical Trial Management Director (ACTMD) (Clinical Research): Leading clinical delivery for large, multi-regional trials and study programs with an accent on recruitment, risk mitigation, quality, project finances, and regulatory compliance. Focus on developing clinical strategies, coordinating cross-functional stakeholders, managing clinical teams, and delivering complex studies under ICH-GCP requirements.

Location: Parsippany, New Jersey, United States of America

Salary: $106,100–$295,500 annual base pay

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Lead clinical delivery for large, multi-regional studies and programs in accordance with contracts, protocols, SOPs, regulatory requirements, and project plans.
  • Set recruitment strategies, monitor recruitment targets, and manage clinical risks throughout the project lifecycle.
  • Develop clinical strategies, quality plans, operational plans, and clinical operation plans for projects and business proposals.
  • Manage clinical project finances, including Estimate at Completion, scope changes, and additional service opportunities.
  • Lead clinical teams, plan resources and talent, provide project-level guidance and training, and support professional development.
  • Coordinate internal and external stakeholders, support milestones, participate in bid defenses, and resolve delivery issues.

Requirements

  • Bachelor’s degree in healthcare or another scientific discipline.
  • At least 10 years of clinical research or monitoring experience, or an equivalent combination of education, training, and experience.
  • In-depth knowledge of Good Clinical Practice and International Conference on Harmonization guidelines.
  • Knowledge of clinical trial conduct, project management practices, project finances, and applicable regulations and local laws.
  • Strong English communication skills, problem-solving ability, planning and prioritization skills, and attention to detail.
  • Leadership, influencing, negotiation, mentoring, training, collaboration, and Microsoft Office skills are required.

Culture & Benefits

  • Full-time employment with health and welfare benefits.
  • Potential incentive plans, bonuses, and other compensation may be available depending on the position.
  • Work involves collaboration across geographies and awareness of cultural differences.
  • Equal opportunity employment and a commitment to integrity in the hiring process.

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