Clinical Trial Supply (CTS) Study Manager — CSL Behring
- Location
- Bern
- Contract
- full-time
- Posted
- 3 days ago
Role overview
Work Environment
This is a hybrid position based onsite at any of the posted locations with a minimum of 3 days onsite weekly.
Relocation and mobility assistance are not provided.
- Work Environment:
- This is a hybrid position based onsite at any of the posted locations with a minimum of 3 days onsite weekly.
- Main Responsibilities:
- Ensure efficient, cost-effective clinical trial supply planning and management for low to medium complexity studies
Main responsibilities
- Main Responsibilities:
- Ensure efficient, cost-effective clinical trial supply planning and management for low to medium complexity studies
- Performs planning and forecasting of drug volume requirements Sample collection and analysis
- Ensures proper storage, transportation and archiving
- Assists with selection and management of external service providers in compliance with outsourcing strategy to ensure cost efficient and high quality services
- Leverages interactive response technology (IRT) system to support clinical supply management activities
- Authors/reviews critical study documents (e.g. study protocol, product dossiers, handling instructions, study reports)
- Leads or participates in global Clinical Trial Supply project meetings with internal and external team members
- Partners with R&D and other functions to ensure optimal use of systems and processes to support clinical trial supply chain
- Supports continuous improvements in clinical drug supply and revises SOPs to ensure ongoing compliance and efficient conduct of clinical trial supply activities Minimum Qualifications:
Application process
- If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement .
Additional details
- Performs planning and forecasting of drug volume requirements Sample collection and analysis
- Supports continuous improvements in clinical drug supply and revises SOPs to ensure ongoing compliance and efficient conduct of clinical trial supply activities Minimum Qualifications:
- Team-player with proven effective interpersonal and communication skills
- To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .
- For more information on CSL benefits visit How CSL Supports Your Well-being | CSL .
- To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging Equal Opportunity Employer
Notes and original content
- Performs planning and forecasting of drug volume requirements
- Sample collection and analysis
- Supports continuous improvements in clinical drug supply and revises SOPs to ensure ongoing compliance and efficient conduct of clinical trial supply activities
- Minimum Qualifications:
- About CSL Behring
- Our Benefits
- You Belong at CSL
- To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging
- Equal Opportunity Employer
Questions about this listing
What salary does CSL Behring offer for this role?
CSL Behring lists CHF 94'500 - 143'000 gross per year for this position in Bern. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does CSL Behring offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with CSL Behring during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Bern?
EU/EFTA residents living in the border zone of the country adjoining Canton Bern can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Bern's cantonal migration office or with HR during the application.
How do I apply for this position at CSL Behring?
Use the "Apply now" button on this page — it links directly to CSL Behring's original listing at csl.wd1.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
