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Senior Manager Clinical Operations; m​/f​/d

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: Fresenius SE & Co. KGaA
Tiempo completo puesto
Publicado en 2026-09-01
Especializaciones laborales:
  • Servicios Médicos
    Administración de Salubridad
Rango Salarial o Referencia de la Industria: 90000 - 120000 EUR Anual EUR 90000.00 120000.00 YEAR
Descripción del trabajo
Puesto: Senior Manager Clinical Operations (m/f/d)

Location:

Spain and Hungary Functional Goal:

Responsible for the strategic and tactical operational planning and execution of R&D sponsored clinical programs for all corporate sponsored programs for Phase I - Phase IV.

Main Tasks:
  • Responsible and accountable for planning, coordinating, overseeing, and conducting complex global clinical trials in one or more therapeutic areas.
  • Collaborate in a global environment, using best practices and knowledge of internal and external business issues to improve processes, standards, and services.
  • Accountable to plan, drive and monitor protocol related activities throughout the lifecycle of the project ensuring targets are met according to timelines, budget and quality expectations.
  • Lead (multiple) cross-functional teams and drive oversight of CRO’s and vendor management and has in-depth business knowledge and strategic understanding of how cross-functional teams jointly achieve objectives and goals of trial team, utilizing knowledge of the organization, processes, customers, and key business drivers to increase effectiveness.
  • Understand the different requirements of agencies related to the clinical packages and plans manages accordingly the different functions (i.e. CSR, TFLs, ISS etc.)
  • Responsible for inspection readiness.
  • Accountable for CAPAS related to clinical programs within the field of Clinical Operations.
  • Accountable and responsible for the financial planning, budget, accruals, forecasts contribution.
  • Preparing clinical program updates and/or contribution to them as needed.
Qualification profile:
  • Advance degree in life sciences (graduate degree), e.g. Biology, Chemistry, Pharmaceuticals preferred or medical background
  • At least 7 years’ experience in clinical research in industry, and at least 5 years in clinical trial management
  • Understanding GxP and global requirements
  • Strong project management skillsets
  • Excellent communication skills and ability to manage cross functional teams
  • Ability to deal with complex situations and drive solution orientated thinking
  • Fluent in English
  • Excellent team player, ability to work under high pressure and pronounced resiliency
  • Experience working in an international and cross-functional team
  • Ability to present and defend the perspective
  • Experienced in Microsoft project, Excel, Power point
Other Tasks:
  • Participate in relevant meetings
  • Plan and set up cross-functional meetings, meetings with vendors and others as needed
  • Own and/or contribute to SOP development /reviews
  • Support sponsor oversight through participation in site visits, including Site Initiation Visits (SIVs) and Co-Monitoring Visits, as required
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Requisitos del puesto
10+ años Experiencia laboral
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