Назад
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2 дня назад

Senior Manager, Clinical Study Lead

150 500 - 245 500$
Формат работы
hybrid/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 Manager, Clinical Study Lead (Clinical Trials): Leading the global execution of large and complex clinical trials in the Inflammation & Immunology area with an accent on study operations, cross-functional leadership, budgets, timelines, and regulatory-compliant delivery. Focus on designing and overseeing study documentation, managing vendors and clinical systems, mitigating operational risks, and supervising clinical trial management staff.

Location: Armonk, NY or Warren, NJ; primarily on-site with hybrid flexibility. Travel of up to 25% may be required.

Salary: $150,500–$245,500 annually.

Company

hirify.global is a biotechnology company that develops and commercializes medicines for serious diseases.

What you will do

  • Lead cross-functional teams responsible for global clinical study delivery from design through closeout.
  • Oversee study documentation, clinical trial systems, monitoring plans, data review, and statistical analysis planning.
  • Identify outsourcing needs and manage vendor engagement, contracting, and performance.
  • Manage study budgets, timelines, risk assessments, feasibility evaluations, patient recruitment, and retention strategies.
  • Monitor site activation, monitoring visits, data entry, query resolution, clinical supplies, and study drug accountability.
  • Supervise Clinical Trial Management staff, including assignments, performance management, recruitment, coaching, mentoring, and training.

Requirements

  • Bachelor’s degree and at least 8 years of relevant clinical trial experience.
  • Experience with line management and strong interpersonal, leadership, negotiation, and stakeholder-influence skills.
  • Extensive experience in global clinical trial operations and contributing to protocols and key study documents.
  • Advanced proficiency with trial management systems and Microsoft applications, including Project, PowerPoint, Word, Excel, IVRS/IWRS, and EDC.
  • Ability to apply advanced expertise and implement operational strategy for clinical studies.

Culture & Benefits

  • Inclusive workplace and equal employment opportunity environment.
  • Comprehensive rewards may include annual incentives, equity awards, retirement benefits, 401(k) matching, insurance, wellness programs, paid time off, and family support benefits.
  • Many roles are performed together on-site, with hybrid flexibility available for this position.

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