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Senior Manager, Site Partnerships EMEA

vor 2 Monaten


Opfikon, Zürich, Schweiz CSL Vifor Vollzeit
About the Role

CSL Vifor is seeking a highly skilled Senior Manager, Site Partnerships EMEA to join our team. As a key member of our Site Partnerships Group, you will play a critical role in positioning CSL as the preferred partner for sites and supporting our clinical pipeline with data-driven decisions.

The ideal candidate will have a strong background in clinical research, with a minimum of 12 years of experience in the pharmaceutical industry. You will be responsible for analyzing data to provide strategic insights into site feasibility, identification, and selection, as well as building and developing strong relationships between CSL and study sites.

Key Responsibilities

  • Analyze data to identify trends and areas for improvement in site relationships and satisfaction.
  • Develop and maintain strong relationships with existing key institutions and partner sites to deliver CSL's portfolio.
  • Establish new sites as Partners in alignment with CSL's portfolio and country strategy.
  • Collect, centralize, analyze, and share information about site relationships with internal stakeholders.
  • Gather essential knowledge about the assigned region, including standard of care, patient pathways, healthcare system, competitive landscape, clinical trial regulations, and patient advocacy groups.

Requirements

  • At least 12 years of relevant clinical research experience within the pharmaceutical industry.
  • At least 4 years of background in Clinical Trial Management, including International Clinical Trial Management for a Sponsor.
  • Proven experience in researching databases and literature, analyzing, interpreting, and presenting data to various stakeholders.
  • Proficiency in advanced MS Office applications, especially Excel and PowerPoint.
  • Experience working in an international environment with building alliances and influence across national and cultural boundaries.
  • Throughout understanding of the drug development process and clinical trial execution.
  • Deep understanding of different needs and goals of Sites, SMOs, CROs, and Sponsors.
  • Ability to work independently and in a fast-paced, hands-on, flexible, dynamically changing environment.
  • Ability to influence organization and cross-functional peers.
  • Works effectively in cross-functional terms.
  • Team building and team-oriented approach.
  • High ethical standards and integrity.
  • Travel Requirements: Ability to travel locally and internationally (up to 20%).

About CSL Vifor

CSL Vifor aims to become the global leader in iron deficiency and nephrology. We are a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology, and rare conditions. We strive to help patients around the world with severe, chronic, and rare diseases lead better, healthier lives.

For more information, please visit viforpharma.com.

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