Global Immunology Clinical Development Strategist
Vor 3 Tagen
CSL Behring is a global biotechnology leader, driven by a commitment to saving and improving lives. Millions of people worldwide live with rare and serious medical conditions, and our company is dedicated to delivering innovative medicines that make a meaningful difference.
With a presence in over 35 countries and a global workforce of approximately 30,000 employees, CSL is inspired to develop and deliver a range of lifesaving therapies for complex disorders such as hemophilia and primary immune deficiencies, as well as vaccines to prevent influenza. Our treatments are also used in cardiac surgery, organ transplantation, and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus, and CSL Vifor, and we are a leading player in the protein biotherapeutics industry.
We are seeking an exceptional Senior Director, Immunology Therapeutic Area, to join our clinical development team. This is a hybrid role, with opportunities to work from our offices in King of Prussia, PA, Bern, Switzerland, or Zurich, Switzerland. You will report to the Global Clinical Lead, Immunology Therapeutic Area.
The Opportunity
As a key member of our clinical development team, you will provide strategic and clinical leadership to assigned programs and individual clinical trials, from conceptualization to execution. Your expertise in Immunology will be instrumental in shaping the clinical development strategy and ensuring the success of our programs.
Key Responsibilities
- Develop and implement clinical development strategies and delivery plans for investigational and marketed products, aligned with the company's Therapeutic Area- and global Product strategy.
- Author and contribute to program and study level documents, as well as educational materials for internal and external trainings, according to the scientific/medical strategy.
- Provide medical oversight of selected products within the Immunology Therapeutic Area and define and implement medical monitoring and oversight strategy for individual clinical studies.
- Collaborate with cross-functional teams to ensure the safe, efficient, and successful execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
Your Qualifications
- MD (Medical Doctor degree) or international equivalent from a recognized school of medicine, plus accredited residency.
- 2+ years minimum experience as a physician in patient care.
- 5+ years pharmaceutical/biotechnology industry experience, with 2 years of accountability for Phase 2b/3 clinical development programs. Relevant academic research experience will also be considered.
- Knowledge of the drug development process, clinical research methodologies, and experience in clinical trial design, data analysis/statistics, and data interpretation.
Benefits
- Medical, dental, and vision coverage.
- 401K plan.
- Paid time off.
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