5 дней назад
Lead, Trial Delivery Management (Clinical Trials)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Lead, Trial Delivery Management (Clinical Trials): Executing study-level activities and coordinating country and regional delivery for global clinical trials with an accent on trial documentation, vendor oversight, feasibility strategy, and risk management. Focus on resolving trial-related issues, supporting regulatory inspections, improving operational processes, and mentoring trial management team members.
Location: High Wycombe, Buckinghamshire, United Kingdom. The role is also available in Spring House and Titusville, United States; Beerse, Belgium; Breda, Netherlands; Warsaw, Poland; Madrid, Spain; and Milan, Italy. Travel up to 15–20% may be required.
Company
Johnson & Johnson MedTech develops healthcare solutions and innovative medicines focused on preventing, treating, and curing complex diseases.
What you will do
- Execute study-level activities and create or update trial-specific documents, including monitoring guidelines, informed consent forms, and investigational medicinal product documentation.
- Set up and oversee vendors, including statements of work, budgets, and day-to-day delivery.
- Coordinate country and regional trial management activities, feasibility strategy, local risk reviews, and operational challenges.
- Support program-level compound training and provide input into trial-level operational strategies.
- Resolve trial issues, mitigate risks, support health authority inspections, and contribute to risk mitigation plans.
- Drive process improvement and mentor or support onboarding for trial management colleagues.
Requirements
- BS degree or equivalent, preferably in life sciences such as biology, chemistry, biochemistry, nursing, or pharmacy.
- At least 4 years of clinical trial experience in pharmaceutical, healthcare, or related industries.
- Operational knowledge across Phase I–IV studies and experience managing multiple aspects of clinical trial execution.
- 2–3 years of experience supporting multiple aspects of global clinical trials.
- Leadership, decision-making, analytical, financial management, project planning, communication, and presentation skills.
- Experience working in multifunctional, matrixed, and global environments, including mentoring or coaching others with limited supervision.
Nice to have
- Experience in pharmaceutical, biopharmaceutical, or biotechnology industries.
Culture & Benefits
- Work within an inclusive environment that values individual contributions, diversity, and dignity.
- Collaborate across Clinical, CTL&D, Medical Writing, local teams, vendors, and global functions.
- Contribute to patient-focused medicines development and healthcare innovation.
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