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Search & Evaluation Late TA Lead, Senior Director (CVR)
full-timeSwitzerland

Summary

Location

Switzerland

Type

full-time

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About this role

Position Description Summary

Three Senior/Executive Directors of Search & Evaluation to lead strategic sourcing and evaluation of later-stage external clinical assets in Immunology, Hematology, and Cardiovascular/Renal therapeutic areas. These leaders will focus on opportunities from Phase 2 through marketed drugs, requiring deep clinical expertise, strong engagement with external Key Opinion Leaders (KOLs) and clinical investigators, and a keen understanding of evolving standards of care. The role is critical to shaping our portfolio through high-impact partnerships and transactions.

Main Responsibilities & Accountabilities

  • Serve as the senior S&E leader within the TALT, influencing therapeutic strategy and integrating late-stage external innovation priorities into portfolio planning.

  • Lead proactive sourcing efforts for Phase 2 to marketed assets, identifying opportunities that align with TA strategy and unmet medical needs.

  • Co-lead internal meetings (with Early Search Lead) focused on evaluating and prioritizing New Product Opportunities (NPOs) within each CSL’s therapeutic areas. NPO meetings are strategic checkpoints where cross-functional teams review potential assets identified by Search and decide whether to advance them for further due diligence and deal negotiations

  • Engage extensively with external KOLs, clinical investigators, and networks to validate asset potential, understand trial designs & clinical endpoints, and anticipate competitive dynamics.

  • Maintain deep awareness of changing standards of care and competitive landscapes to inform sourcing priorities and deal strategy.

  • Drive cross-functional due diligence for late-stage assets, coordinating clinical, regulatory, commercial, and market access assessments to support governance decisions.

  • Partner closely with BD and Regional Ecosystem Leads to advance high-priority opportunities through negotiation and deal close, ensuring seamless handoff and execution

  • Represent the TA externally, leading sourcing activities at specialized conferences and building relationships with pharma, biotech, and clinical communities.

Qualifications & Experience Requirements

  • 15+ years in biopharma with significant experience in clinical development, external innovation, or business development.

  • Advanced degree required (MD, PhD, or equivalent).

  • Deep clinical expertise in Immunology, Hematology, or Cardiovascular/Renal therapeutic areas.

  • Proven track record of sourcing and closing late-stage deals and engaging with KOLs and clinical networks.

  • Strong understanding of regulatory pathways, market access, and competitive standards of care.

About CSL Plasma

CSL Plasma operates one of the world’s largest and most sophisticated plasma collection networks, with over 350 plasma collection centers in the U.S., Europe and China. Headquartered in Boca Raton, Florida, CSL Plasma is a subsidiary of CSL Behring, a global biotherapeutics business and a member of CSL. Plasma collected at CSL Plasma facilities is used by CSL Behring for the sole purpose of manufacturing lifesaving plasma-derived therapies for people in more than 100 countries. The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people.

Learn more about CSL Plasma here https://www.cslplasma.com/ and CSL, CSL Behring, CSL Seqirus and CSL Vifor here https://www.csl.com/.

Learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor here at https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

 

Our Benefits

For more information on CSL Plasma benefits visit https://cslbenefits.com/cslp.

 

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

 To learn more visit https://www.csl.com/careers/inclusion-and-belonging

 

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

Other facts

Tech stack
Clinical Development,External Innovation,Business Development,Immunology,Hematology,Cardiovascular,Renal Therapeutic Areas,Sourcing,KOL Engagement,Regulatory Pathways,Market Access,Competitive Standards,Portfolio Planning,Due Diligence,Negotiation,Deal Closing

About CSL

CSL Plasma is one of the world’s largest collectors of human plasma. We are committed to excellence and innovation in everything we do. Our work ensures that tens of thousands of people with rare and serious diseases are able to live normal, healthy lives. We are committed to our work because people’s lives depend on us. See our community guidelines: https://bit.ly/2IApjpz.

Supported by parent company CSL Behring, the global leader in plasma protein biotherapeutics, CSL Plasma has more than 280 plasma collection centers globally. CSL Plasma also has a state-of-the-art testing laboratory that features some of the most advanced technology, instrumentation and automation in the field; two logistics centers, one in Dallas and one in Indianapolis. Our corporate headquarters in Boca Raton, Florida.

Our U.S. plasma collection centers are committed to the highest standards of quality and safety. When you donate, you give a valuable gift to those who require plasma-derived therapies to live healthier lives.

The CSL Group has a combined heritage of outstanding contribution to medicine and human health with more than 100 years experience in the development and manufacture of vaccines and plasma protein biotherapies.

With major facilities in Australia, Germany, Switzerland and the US, CSL has over 30,000 employees working in more than 35 countries. See our community guidelines: https://bit.ly/3QZbZeZ

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing

What you'll do

  • The Senior Director will lead strategic sourcing and evaluation of later-stage external clinical assets, focusing on opportunities from Phase 2 through marketed drugs. This role involves engaging with KOLs and clinical investigators to validate asset potential and drive cross-functional due diligence.

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Frequently Asked Questions

What does a Search & Evaluation Late TA Lead, Senior Director (CVR) do at CSL?

As a Search & Evaluation Late TA Lead, Senior Director (CVR) at CSL, you will: the Senior Director will lead strategic sourcing and evaluation of later-stage external clinical assets, focusing on opportunities from Phase 2 through marketed drugs. This role involves engaging with KOLs and clinical investigators to validate asset potential and drive cross-functional due diligence..

Why join CSL as a Search & Evaluation Late TA Lead, Senior Director (CVR)?

CSL is a leading Pharmaceutical Manufacturing company.

Is the Search & Evaluation Late TA Lead, Senior Director (CVR) position at CSL remote?

The Search & Evaluation Late TA Lead, Senior Director (CVR) position at CSL is based in Switzerland, Switzerland. Contact the company through Clera for specific work arrangement details.

How do I apply for the Search & Evaluation Late TA Lead, Senior Director (CVR) position at CSL?

You can apply for the Search & Evaluation Late TA Lead, Senior Director (CVR) position at CSL directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about CSL on their website.