Associate Director, Clinical Development, Immunoglobulins (m/w/x)

For our Clinical Development department, we are looking for a clinical scientist

R-245333

Fulltime / permanent/ non-tariff

As Associate Director, Clinical Development, Immunoglobulins you will be responsible for key scientific input to clinical development strategies and therapeutic areas and report to the Director of Global Clinical Science Lead

The Opportunity

• Provides innovate scientific and clinical development leadership for the safe, efficient and timely execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
• Will be a leader in the development of the scientific strategy of the clinical development plan, the design and development of trial related documents and the scientific oversight of clinical trials. Leads a team to oversee and guide the clinical strategy within projects and programs.
• Defines scientific strategy for critical program components.
• Can lead development of Clinical Development Program.
• Guides development of clinical study demounts and development/critical review of submission documents.
• Guides concept and review of manuscripts, conference abstracts, etc.
• Collaboratively develops the clinical development strategy with project teams, providing input, guidance and mentorship for project teams.
• Leads the scientific analysis and interpretation of clinical data and the writing of clinical study reports, internal and external scientific meeting presentations and peer-reviewed publications, and all regulatory submission documents.
• Will have a key role in fostering close collaboration with other departments, defining and improving interfaces to other functions, developing and mentoring scientists at all levels

Your Skills and Experience

• Bachelor degree or equivalent in Science, Allied Health or Engineering.
• Preferred: An advanced degree (MSc, PhD) in Science, Allied Health or Engineering, PMP Certification, Masters of Business Administration (MBA) or equivalent.
• 8-10 years experience in the biotechnology or pharmaceutical industry (or where relevant a biomedical research organization).
• At least five years experience in managing projects.
• In-depth knowledge in the drug development and manufacturing processes for pharmaceuticals (CMC, non-clinical, clinical, Regulatory Affairs).
• Experience in Clinical Development is an advantage

What we offer

• Excellent income potential and extended benefits
• Two additional leave days for your personal wellbeing
• Family services such as psychological support, legal advice, family care services and more for you and your direct family
• Hybrid working models

For more information, please check out our global benefits below

We are looking forward to your application. Please ensure to apply online with your CV and certifications as well as your salary expectation.

We encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

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