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3 дня назад

Associate Clinical Trial Management Director (ACTMD) (Clinical Trials)

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 Trials): Leading clinical delivery for large, multi-regional studies and clinical programs with an accent on recruitment, risk mitigation, quality compliance, project finances, and stakeholder management. Focus on developing clinical strategies, coordinating cross-functional teams, managing delivery risks and budgets, and mentoring clinical leads across global trials.

Location: Durham, North Carolina, United States of America

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

Company

IQVIA 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.
  • Manage recruitment strategies, clinical risks, quality standards, compliance monitoring, and issue resolution throughout the project lifecycle.
  • Develop clinical strategies and operational plans, including project finance plans, Estimate at Completion management, and scope-change oversight.
  • Lead clinical teams, coordinate with Project Leaders and functional teams, manage stakeholders, and support project milestones.
  • Plan clinical team resources, provide project guidance and training, and support professional development through feedback, mentoring, and coaching.
  • Contribute to business proposals, bid defense activities, clinical operations plans, cross-functional initiatives, and site visits when applicable.

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 ICH Good Clinical Practice and applicable clinical research regulations, laws, and guidelines.
  • Consolidated knowledge of project management practices, project finances, planning, prioritization, and risk management.
  • Strong written and verbal communication, problem-solving, leadership, negotiation, mentoring, and collaboration skills.
  • Good command of English is required. Proficiency with Microsoft Word, Excel, PowerPoint, and other software systems is also required.

Culture & Benefits

  • Work within a global clinical research and healthcare intelligence organization.
  • Collaborate across geographies with awareness of cultural differences.
  • Support innovative medical treatment development and improved patient outcomes.
  • Health and welfare benefits may be provided in addition to base pay.
  • Incentive plans, bonuses, or other compensation may be available depending on the position.

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