4 дня назад
Trial Delivery Manager, Sponsor Dedicated (Clinical Trial Management)
93 100 - 295 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →
Похожие вакансии
8 дней назад
Senior Manager, Clinical Study Lead
150 500 - 245 500$
10 дней назад
Clinical Project Manager II / Senior Clinical Project Manager (Biopharmaceutical)
11 дней назад
Lab Operations Manager (Clinical Trials)
100 564 - 136 058$
4 дня назад
Project Manager (Clinical Research)
9 дней назад
Remote Visit Coordinator, US Regional Specialist
51 000 - 127 400$
6 дней назад
Associate Director, Clinical Supplies Project Manager (Clinical Supplies)
142 500 - 256 500$