2 дня назад
Senior Clinical Project Manager (Clinical Trials)
52 000 - 65 000€
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Clinical Project Manager (Clinical Trials): Coordinating the operational management of clinical trials and developing compounds in line with medical and scientific standards with an accent on CRO oversight, study documentation, clinical trial supplies, risk management, and budget control. Focus on managing complex clinical studies, ensuring ICH/GCP and SOP compliance, coordinating study deliverables, and presenting clinical results.
Location: Based at the headquarters in Parma, Italy; flexible hybrid and predominantly remote working arrangements are available.
Salary: €52,000–€65,000 per year, plus eligibility for an annual bonus.
Company
is an international research-focused biopharmaceutical group operating in more than 30 countries, with R&D activities across clinical development, regulatory affairs, pharmacovigilance, quality assurance, and project and portfolio management.
What you will do
- Coordinate the operational management of 1–3 clinical trials across different phases and therapeutic areas.
- Manage CROs, clinical providers, internal stakeholders, study teams, and vendor activities.
- Review project, monitoring, risk management, and site-related documents and maintain the study risk register.
- Manage clinical operations documentation in the electronic Trial Master File and coordinate investigators’ meetings, safety boards, data reviews, and other scientific meetings.
- Coordinate clinical study reports, study results presentations, clinical trial supplies, corrective and preventive actions, and audit follow-ups.
- Prepare, present, and control study budgets while ensuring delivery within scope, timelines, budget, quality standards, and SOPs.
Requirements
- At least 3 years of experience in a similar position in a pharmaceutical company.
- Successful planning and execution of at least 5 clinical studies.
- Degree in Life Sciences, pharmacy, biological sciences, another health-related discipline, or equivalent.
- Fluent English required.
- Knowledge of clinical study design, clinical research statistics, planning tools, ICH/GCP, company SOPs, and GLP for bioanalytical assays.
- Current knowledge of relevant clinical research literature.
Culture & Benefits
- Flexible hybrid and remote work options.
- Annual performance bonus eligibility.
- Pension, private medical insurance, wellbeing programs, and flexible benefits.
- Work-life balance initiatives, training, development resources, and tax assistance services for foreign colleagues.
- Relocation support is available.
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