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
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)
Education and skills
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
Further information can be found below under ‘What we offer’
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 (https://www.cslbehring.de/karriere/was-wir-bieten) 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 (https://www.cslbehring.de/unser-unternehmen) .
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 (https://www.csl.com/careers/inclusion-and-belonging) at CSL.
Do work that matters at CSL Behring!
R-253043
CSL makes all employment decisions without regard to race, color, religion, national origin, ancestry, age, sex, gender, pregnancy, disability, marital status, sexual orientation, gender identity, genetic information, military status, protected veteran status (specifically status as a disabled veteran, recently separated veteran, armed forces service medal veteran, or active duty wartime or campaign badge veteran) or other classification protected by applicable US federal, state or local law. CSL complies with all applicable employment laws, including but not limited to Title VII of the Civil Rights Act of 1964, the Americans with Disabilities Act, the Fair Labor Standards Act, and the Immigration Reform and Control Act. https://www.cslbehring.com/careers/eeo-statement