Associate Director, Clinical Development, Immunoglobulins (m/w/x)
Publication date:
25 October 2024Workload:
100%- Place of work:EMEA, DE, Marburg, CSL Behring
For our Clinical Development department, we are looking for a clinical scientist
Associate Director, Clinical Development, Immunoglobulins (m/f/x)
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.
Was wir bieten
Wir möchten, dass Sie sich bei CSL wohl fühlen. Das ist wichtig und Sie sind es auch. Erfahren Sie mehr darüber, was wir bei CSL bieten .
Über CSL Behring
CSL Behring ist ein weltweit führendes Unternehmen, das hochwertige Therapeutika für Menschen mit seltenen und ernsten Krankheiten entwickelt und vertreibt. Mit unseren Medikamenten für die Therapiegebiete Immunologie, Hämatologie, Herz-Kreislauf und Stoffwechsel, Atemwegserkrankungen und Transplantationsmedizin halten wir unser Versprechen, die Lebensqualität von Patienten in mehr als 100 Ländern zu verbessern. Erfahren Sie mehr über CSL Behring .
Wir möchten, dass CSL so bunt ist wie die Welt, in der wir leben
Als globales Unternehmen mit Mitarbeitenden in über 35 Ländern steht CSL für Vielfalt, Fairness und Inklusion. Erfahren Sie mehr über Vielfalt, Fairness & Inklusion bei CSL.