Global Principal Clinical Scientist - Cardiorenal — CSL Behring
NewCHF 101'500 - 154'000
CSL Behring · Glattbrugg (ZH)
- Location
- Glattbrugg
- Contract
- full-time
- Posted
- Yesterday
SalaryCHF 101'500 - 154'000
Role overview
- You will be responsible for scientific input to clinical development strategies and therapeutic areas.
- Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
- Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial related documents and the scientific oversight of clinical trials.
- You will facilitate a team to define and deliver the clinical strategy within programs.
- Define scientific strategy for multiple program components.
- You will lead the development of Clinical Development Program.
- Author clinical study documents and assists with development/critical review of submission documents.
- Contribute to authorship and review of manuscripts and conference abstracts.
- Collaboratively develop the clinical development strategy with project teams, providing input, guidance and mentorship for project teams.
- Contribute to 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.
- You will be responsible for scientific input to clinical development strategies and therapeutic areas.
- Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
- Bachelor's degree or equivalent in Science, Allied Health or Engineering.
Main responsibilities
- You will be responsible for scientific input to clinical development strategies and therapeutic areas.
- Provide scientific and clinical development input for the safe and efficient execution of assigned programs, ensuring the highest quality and full compliance of all outputs.
- Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial related documents and the scientific oversight of clinical trials.
- You will facilitate a team to define and deliver the clinical strategy within programs.
- Define scientific strategy for multiple program components.
- You will lead the development of Clinical Development Program.
- Author clinical study documents and assists with development/critical review of submission documents.
- Contribute to authorship and review of manuscripts and conference abstracts.
- Collaboratively develop the clinical development strategy with project teams, providing input, guidance and mentorship for project teams.
- Contribute to 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.
Key requirements
- Bachelor's degree or equivalent in Science, Allied Health or Engineering.
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 .
Company and context
- 8+ years experience in the biotechnology or pharmaceutical industry (or where relevant a biomedical research organization).
- 5+ years managing projects.
- In-depth knowledge in the drug development and manufacturing processes for pharmaceuticals (CMC, non-clinical, clinical, Regulatory Affairs).
- The role is based in Glattbrugg, Switzerland and requires an onsite presence of 3 days per week. About CSL Behring
- CSL Behring is a global biotherapeutics leader driven by our promise to save lives.
- Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
- We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
- CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma.
- Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
- 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/ . Our Benefits
Additional details
- The role is based in Glattbrugg, Switzerland and requires an onsite presence of 3 days per week.
- 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
- Responsibilities:
- 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 101'500 - 154'000 gross per year for this position in Glattbrugg. 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 Zürich?
EU/EFTA residents living in the border zone of the country adjoining Canton Zürich 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 Zürich'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.
