5 дней назад
Lead, Trial Delivery Management
64 000 - 103 040€
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 planning, and risk management. Focus on resolving operational issues, supporting health authority inspections, improving trial processes, and mentoring trial management colleagues.
Location: Breda, Netherlands; also available in Belgium, Spain, Italy, Poland, the United Kingdom, and the United States. Travel up to 15–20% may be required.
Salary: €64,000–€103,040 annually in the primary posting location. Additional ranges vary by country.
Company
Johnson & Johnson develops healthcare, pharmaceutical, and MedTech solutions 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 manage study vendors, including statements of work, budgets, and day-to-day delivery.
- Coordinate country and regional trial management activities, feasibility strategy, target setting, and country-level risk reviews.
- Support compound training and provide input into trial-level operational strategies.
- Resolve trial issues, define risk mitigation plans, and support health authority inspections.
- Drive process improvement and mentor or support onboarding for colleagues in Trial Management.
Requirements
- Bachelor’s 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 a related industry.
- Operational knowledge across Phase I–IV studies and the ability to manage multiple aspects of clinical trial execution.
- 2–3 years of experience supporting multiple aspects of a global clinical trial.
- 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.
Nice to have
- Experience in pharmaceutical, biopharmaceutical, or biotechnology industries.
- Knowledge of clinical trial management systems, clinical trial design, laboratory operations, quality assurance, regulatory compliance, SOPs, and research ethics.
Culture & Benefits
- Inclusive work environment focused on individual contribution, diversity, and dignity.
- Annual bonus or sales commissions may be available depending on pay grade, location, and performance.
- Vacation, parental leave of at least 12 weeks, bereavement leave, caregiver leave, and volunteer leave.
- Well-being reimbursement and programs supporting financial, physical, and mental health.
- Recognition awards and access to insurance plans subject to local eligibility and plan terms.
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