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4 дня назад

Trial Delivery Manager, Sponsor Dedicated (Clinical Trial Management)

93 100 - 295 500$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior/lead
Английский
c1
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
Trial Delivery Manager, Sponsor Dedicated (Clinical Trial Management): Leading centralized oversight and delivery of complex global clinical trials across feasibility, start-up, execution, database lock, and close-out with an accent on vendor governance, inspection readiness, and risk management. Focus on coordinating Study Management Teams, driving enrollment and operational milestones, and resolving quality, compliance, budget, and delivery challenges across global stakeholders.

Location: Home-based remote role on the East Coast, United States

Annual base pay: $93,100–$295,500, with potential additional incentives, bonuses, and benefits.

Company

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

What you will do

  • Lead global and regional clinical trial management activities across internally managed and outsourced studies.
  • Coordinate Study Management Teams and serve as a central point of contact for country, regional, functional, and global stakeholders.
  • Drive trial delivery from feasibility and site selection through start-up, execution, database lock, and close-out.
  • Oversee CROs and vendors supporting IWRS/IVRS, central laboratories, ePRO/eCOA, imaging, translations, supplies, and investigator meetings.
  • Maintain trial oversight through dashboards, reporting, issue tracking, risk management, and enrollment planning.
  • Support inspection readiness, CAPA resolution, audits, regulatory submissions, documentation, and continuous process improvement.

Requirements

  • Bachelor’s degree or equivalent in Life Sciences, such as Biology, Chemistry, Nursing, or Pharmacy.
  • At least 6 years of clinical trial management experience for the base level, or 8+ years including leadership of complex global studies for the advanced level.
  • Experience managing trials from start-up through database lock and close-out, including 2–3+ years coordinating global virtual teams in a large matrix environment.
  • Therapeutic area experience and deep knowledge of ICH-GCP, regulatory requirements, and clinical operations.
  • Experience with project planning, risk mitigation, budgets, CTMS, TMF systems, and Microsoft applications.
  • Fluent English required; local language proficiency may be required depending on the assignment. Willingness to travel as needed.

Nice to have

  • Monitoring experience or equivalent central monitoring or data management experience.
  • Advanced-level experience as a Therapeutic Area Expert or Functional Champion.

Culture & Benefits

  • Home-based remote work on the East Coast.
  • Work in a global, matrixed clinical research environment with cross-functional and virtual teams.
  • Opportunities to mentor team members and contribute to task forces and process improvement initiatives.
  • Potential incentive plans, bonuses, and health and welfare benefits in addition to base pay.

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