Region Zug Zürich Hybrid
For a growing biopharmaceutical development organization in the ZugZurich region we are looking for a Clinical Quality Assurance Specialist / Expert to support the quality oversight of clinical development programs.
This role is suited for early to mid-career professionals with experience in clinical trials and GCP-based quality environments. It is a hands-on specialist role without management responsibility.
Responsibilities
- Support clinical quality oversight of clinical trials
- Review clinical study documentation and processes
- Contribute to Trial Master File (TMF) quality and documentation management
- Support GCP compliance across clinical programs
- Conduct quality reviews and checks of clinical documentation
- Collaborate with Clinical Operations QA and external partners (e.g. CROs)
Profile
- Degree in Life Sciences (BSc or MSc)
- Approx. 37 years of experience in pharma biotech CRO or clinical research
- Experience in Clinical QA Clinical Operations or clinical study environments
- Good understanding of GCP and clinical trial documentation
- Structured pragmatic working style
- Fluent English
Backgrounds of interest
- Clinical QA professionals in pharma or biotech
- Clinical Operations professionals with QA exposure
- CRO professionals with experience in study quality GCP compliance and documentation
- QA specialists with experience in clinical trial oversight or TMF management
- Professionals from clinical study sites with strong experience in study documentation and regulatory requirements
Help shape the future of biosimilars!
Join a growing clinical development organization with a dynamic start-up-like environment and contribute to the quality and compliance of international clinical trials.
Region Zug Zürich HybridFor a growing biopharmaceutical development organization in the ZugZurich region we are looking for a Clinical Quality Assurance Specialist / Expert to support the quality oversight of clinical development programs.This role is suited for early to mid-career professionals w...
Region Zug Zürich Hybrid
For a growing biopharmaceutical development organization in the ZugZurich region we are looking for a Clinical Quality Assurance Specialist / Expert to support the quality oversight of clinical development programs.
This role is suited for early to mid-career professionals with experience in clinical trials and GCP-based quality environments. It is a hands-on specialist role without management responsibility.
Responsibilities
- Support clinical quality oversight of clinical trials
- Review clinical study documentation and processes
- Contribute to Trial Master File (TMF) quality and documentation management
- Support GCP compliance across clinical programs
- Conduct quality reviews and checks of clinical documentation
- Collaborate with Clinical Operations QA and external partners (e.g. CROs)
Profile
- Degree in Life Sciences (BSc or MSc)
- Approx. 37 years of experience in pharma biotech CRO or clinical research
- Experience in Clinical QA Clinical Operations or clinical study environments
- Good understanding of GCP and clinical trial documentation
- Structured pragmatic working style
- Fluent English
Backgrounds of interest
- Clinical QA professionals in pharma or biotech
- Clinical Operations professionals with QA exposure
- CRO professionals with experience in study quality GCP compliance and documentation
- QA specialists with experience in clinical trial oversight or TMF management
- Professionals from clinical study sites with strong experience in study documentation and regulatory requirements
Help shape the future of biosimilars!
Join a growing clinical development organization with a dynamic start-up-like environment and contribute to the quality and compliance of international clinical trials.
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