5 дней назад
Clinical Partnership Manager (Biopharma)
52 240€
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Partnership Manager (Biopharma): Managing strategic CRO partnerships and vendor governance for outsourced clinical trials with an accent on operational excellence, quality delivery, and cross-functional collaboration. Focus on negotiating clinical trial budgets, implementing vendor governance models, resolving process issues, and integrating digital platforms across complex international stakeholder environments.
Location: Based at the R&D Center in Parma, Italy, with hybrid office and remote working
Salary: Minimum €52,240 per year, plus eligibility for an annual performance bonus.
Company
is an international research-focused biopharmaceutical group operating in more than 30 countries and developing innovative medicines across multiple therapeutic areas.
What you will do
- Develop and manage strategic, trust-based partnerships with CROs, vendors, and other external clinical-study providers.
- Maintain and continuously improve the operational and partnership model within Global Clinical Operations.
- Define third-party vendor governance, oversee vendor panels, and monitor timelines, quality, delivery performance, and issue resolution.
- Collaborate with Procurement on Master Service Agreements, Service Level Agreements, and related contractual documentation.
- Partner with study teams and strategic providers on RFP revisions, change orders, BDMs, KOMs, and other study-level interactions.
- Support vendor qualification with Quality Assurance and contribute to new processes, procedures, digital platforms, and continuous-improvement initiatives.
Requirements
- 8–10 years of relevant experience in Clinical Operations, including knowledge of clinical trial management and clinical development phases.
- Experience managing CRO, vendor, or other third-party partnerships involved in clinical studies.
- Experience with vendor governance and performance management, including service quality, delivery performance, and issue resolution.
- Proven experience in clinical trial budget negotiation and management.
- Knowledge of ICH-GCP principles and operational and quality requirements for outsourced clinical trials.
- Fluent English, written and spoken, with the ability to work in an international environment.
Culture & Benefits
- Work in a research-focused, international biopharmaceutical organization and certified B Corp.
- Hybrid working combining office presence and remote work.
- Annual performance bonus scheme and flexible benefits programme.
- Pension, private medical insurance, healthcare programmes, and wellbeing initiatives.
- Development resources, training, work-life balance initiatives, relocation support, and tax assistance for foreign colleagues.
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