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3 дня назад

Director, Clinical Project Management (Oncology)

125 900 - 350 900$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US

Описание вакансии

Текст:
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TL;DR
Director, Clinical Project Management (Oncology) (Clinical Trials): Directing complex global, full-service, multi-regional oncology studies and programs with an accent on operational delivery, strategic decision-making, quality, and financial performance. Focus on leading cross-functional teams, managing strategic risks and customer relationships, and solving delivery, scope, and compliance challenges across the clinical trial lifecycle.

Location: Durham, North Carolina, United States of America

Annual base pay: $125,900.00–$350,900.00. Incentive plans, bonuses, and benefits may also be offered.

Company

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

What you will do

  • Direct the delivery of complex, global, full-service, multi-regional clinical studies and programs from pre-award through close-out.
  • Develop project delivery strategies, contribute to RFPs, and lead bid defense presentations for large and complex programs.
  • Build and lead cross-functional project teams, set objectives, monitor performance, and support milestone achievement.
  • Manage strategic risks, quality issues, corrective and preventive action plans, scope changes, and project escalations.
  • Own customer relationships, serve as the primary project or program contact, and communicate progress to internal and external stakeholders.
  • Ensure project financial success, forecast opportunities, promote best practices, and mentor less experienced project team members.

Requirements

  • Bachelor’s degree in life sciences or a related field, or an equivalent combination of education, training, and experience.
  • At least 12 years of relevant experience, including a minimum of 8 years in project management or a related functional area.
  • Extensive knowledge of clinical trial conduct, ICH GCP, and applicable local laws, regulations, and guidelines.
  • Broad protocol and therapeutic knowledge, strong problem-solving and presentation skills, and demonstrated ability to lead through others.
  • Experience with project financials, contractual obligations, customer management, cross-functional collaboration, and performance mentoring.
  • Strong written and verbal English communication skills required. Proficiency with Microsoft Word, Excel, PowerPoint, and other standard office software is expected.

Culture & Benefits

  • Work with global, cross-functional teams across geographies and cultures.
  • Opportunities to support professional development, mentoring, and knowledge sharing.
  • Health and welfare benefits may be available depending on the position and employment terms.
  • Additional incentive plans, bonuses, or other compensation may be offered.