The primary goal of the newly established Site Partnerships Group is to position CSL as the preferred partner for sites and supporting our clinical pipeline with data to help the organization to make data driven decisions. Reporting to the Director, Site Partnerships, the Senior Manager, Site Partnerships EMEA has two main responsibilities: 1. Maintain existing and develop new strong relationships between CSL and study sites, to position CSL as a priority sponsor. 2. Strengthen and enable internal capacities to support study execution. 3. Support internal pharma intelligence by analyzing, interpreting, and visualizing data from different resources.

Key Tasks & Responsibilities

• Develop and maintain strong relationships with existing key institutions and partner sites to deliver CSL’s portfolio.

• Responsible for establishing new sites as Partner in alignment with CSL’s portfolio and country strategy by working with local stakeholders (e.g., medical directors, country affiliates, MSLs) on new site recommendations, evaluation, and selection.

• Liaise with internal stakeholders, especially with local Medical Affairs, local Affiliates and MSLs, to develop an integrated site engagement strategy to support study execution.

• Collect, centralize, analyze, and share information about site relationships with internal stakeholders. Assess the satisfaction of key sites/institutions in the assigned region regarding their experience interacting and working with CSL. Analyze data to identify trends and areas for improvement.

• Gather essential knowledge about the assigned region, such as standard of care, patient pathways, healthcare system, competitive landscape, clinical trial regulations and patient advocacy groups.

• By analyzing data provide strategic insights into site feasibility, identification and selection, and global patient recruitment strategies.

Your Profile

• At a minimum graduate degree in life science, pharmacy, medical laboratory technology, or other health/medical related area is a must, advanced degree e.g. PhD, PharmD preferred. Other degrees and certifications considered if commensurate with related clinical research experience (e.g., diploma or associate degree RN, certified medical technologist).

• 10+ years’ relevant clinical research (or related, e.g. Medical Affairs, MSL) experience within the pharmaceutical industry/ CRO

• At least 2 years 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.

• 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.

Are you interested in this exciting opportunity? We look forward to receiving your online application.

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

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