Senior Study Specialist (m/f/x) - Clinical Trial Supply
Behringwerke AG
Datum: vor 1 Woche
Stadt: Marburg an der Lahn, Hesse
Vertragstyp: Ganztags
For our Global Supply Chain (Clinical Trial Supply) division we are currently looking for a
Senior Study Specialist (m/f/x) - Clinical Trial Supply
R-253043
Fulltime / Permanent
Multiple locations and hybrid working models available
Tasks and responsibilities
Please apply online with your complete application documents (CV and references) as well as your salary expectations and your notice period.
We look forward to receiving your application!
Our Benefits
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.
About CSL Behring
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 .
We want CSL to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.
Do work that matters at CSL Behring!
Senior Study Specialist (m/f/x) - Clinical Trial Supply
R-253043
Fulltime / Permanent
Multiple locations and hybrid working models available
Tasks and responsibilities
- Planning, implementation and monitoring of a logistics network for assigned simple global clinical trials, including:
- Coordination of worldwide trial supply with internal global departments and external service providers
- Participation in or, if necessary, leading meetings with internal and external expert groups for the provision of clinical trial supplies
- Collaboration on complex global studies in coordination with the supervisor
- Implementation and monitoring of the entire trial supply chain at the study sites, including:
- Creation and revision of study documents
- Training of internal and external stakeholders regarding the handling of the respective product
- Ensuring the SOP-compliant execution of all assigned clinical study activities
- Collaboration in the preparation, execution and follow-up of audits and inspections
- Collaboration in the creation and revision of study-specific software specifications in an IRT system (Interactive Response System)
- Calculation and monitoring of the budget for assigned studies
- Technical collaboration in cross-country and cross-functional projects (e.g. continuous improvement with regard to clinical trials). continuous improvement in relation to clinical trial goods management)
- Bachelor of Science degree, e.g. biology or logistics
- At least 4-5 years of professional experience in clinical research and logistics in the biopharmaceutical industry
- Additional experience in global project management, ideally in an R&D environment
- Knowledge and experience in GCP/cGMP/GDP/ICH
- Fluency in English
- Good presentation skills
Please apply online with your complete application documents (CV and references) as well as your salary expectations and your notice period.
We look forward to receiving your application!
Our Benefits
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.
About CSL Behring
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 .
We want CSL to reflect the world around us
As a global organisation with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL.
Do work that matters at CSL Behring!