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5 дней назад

Clinical Partnership Manager (Biopharma)

52 240
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
France/UK/US +4 еще
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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 hirify.global 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

hirify.global 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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