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3 дня назад

Senior Clinical Trial Manager (Oncology, Sponsor Dedicated)

68 400 - 232 800$
Формат работы
onsite
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 Clinical Trial Manager (Oncology, Sponsor Dedicated) (Oncology clinical research): Leads country-level execution of complex oncology clinical trials, covering site selection, recruitment, compliance, safety, vendor oversight, and budget delivery with an accent on quality, regulatory adherence, and operational risk management. Focus on coordinating matrix teams, resolving site and data-quality issues, maintaining inspection readiness, and driving corrective and preventive actions across high-priority studies.

Location: Durham, North Carolina, United States of America

Salary: $68,400–$232,800 annualized base pay

Company

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

What you will do

  • Lead country-level planning and execution for complex oncology clinical trials, including site selection, feasibility, recruitment, and performance optimization.
  • Act as the primary country-level sponsor contact and coordinate local study teams, investigators, vendors, and external partners.
  • Manage trial compliance, patient safety reporting, data quality, CAPA activities, and inspection readiness across CTMS and eTMF systems.
  • Oversee country-level budgets, forecasting, invoices, vendor performance, and delivery within financial targets.
  • Coordinate informed consent documentation, IEC/HA approvals, local regulatory activities, and country-specific trial requirements.
  • Train, mentor, and support Site Managers and less experienced clinical trial team members.

Requirements

  • BA/BS degree in a health- or science-related field.
  • 3 to 5+ years of trial management experience, including independent management of complex clinical trials and country-level execution.
  • Oncology clinical research experience.
  • Strong knowledge of ICH-GCP, sponsor SOPs, local laws and regulations, protocols, and study procedures.
  • Strong IT skills with relevant software and sponsor systems.
  • Proficiency in English and the applicable country language; willingness to travel occasionally with overnight stays.

Culture & Benefits

  • Equal opportunity employment environment.
  • Health and welfare benefits may be provided depending on the position.
  • Incentive plans, bonuses, or other compensation may be available depending on the position.
  • Work includes collaboration with matrix clinical teams, external partners, investigators, and local stakeholders.

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