Senior Manager, Site Partnerships EMEA

vor 3 Wochen

Opfikon, Zürich, Schweiz CSL Vifor Vollzeit
About the Role

We are seeking a highly skilled Senior Manager, Site Partnerships EMEA to join our team at CSL Vifor. 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.

Key Responsibilities
  • Analyze and interpret data from various resources to provide strategic insights into site feasibility, identification, and selection, as well as global patient recruitment strategies.
  • 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 by working with local stakeholders on new site recommendations, evaluation, and selection.
  • Collect, centralize, analyze, and share information about site relationships with internal stakeholders, assessing the satisfaction of key sites/institutions in the assigned region regarding their experience interacting and working with CSL.
  • 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
  • A minimum graduate degree in life science, pharmacy, medical laboratory technology, or other health/medical-related area is a must; an advanced degree, such as a PhD or PharmD, is preferred.
  • 12+ years of relevant clinical research (or related) 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/or literature, analyzing, interpreting, and presenting data to various stakeholders, including Senior Leadership.
  • 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.
  • A deep understanding of the drug development process and clinical trial execution.
  • 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. The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology, and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic, and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing, and developing, manufacturing, and marketing pharmaceutical products for precision patient care.

For more information, please visit viforpharma.com.

We want CSL to reflect the world around us

As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

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