and applicable local/international regulations, including data protection legislation.
• Conduct feasibility, site selection, initiation, monitoring, and close-out visits at investigational sites.
• Collaborate with Regulatory Affairs and Clinical Operations...
Your new company
Our client is a leading company in the Pharma Sector.
We are seeking a Senior Clinical Research Associate to join our team
You new role
• Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations...
standards, and applicable local/international regulations, including data protection legislation.
Conduct feasibility, site selection, initiation, monitoring, and close-out visits at investigational sites.
Collaborate with Regulatory Affairs and Clinical...
Your new company
Our client is a leading company in the Pharma Sector.
We are seeking a Senior Clinical Research Associate to join our team
You new role
• Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations...
and overall budget; Responsible for management of the Clinical CRO/Providers Acting as primary contact for Clinical (CRO) but also internal customers. Ensures adherence to scope of work within timelines and budget. Performs co-monitoring when needed, as...
works and overall budget; - Responsible for management of the Clinical CRO/Providers Acting as primary contact for Clinical (CRO) but also internal customers. Ensures adherence to scope of work within timelines and budget. Performs co-monitoring when...
Your new company
Our client is a leading company in the Pharma Sector.
We are seeking a Senior Clinical Research Associate to join our team
You new role
Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations
Train...
for management of the Clinical CRO/Providers Acting as primary contact for Clinical (CRO) but also internal customers. Ensures adherence to scope of work within timelines and budget. Performs co-monitoring when needed, as specified in SOP...
works and overall budget; Responsible for management of the Clinical CRO/Providers Acting as primary contact for Clinical (CRO) but also internal customers. Ensures adherence to scope of work within timelines and budget. Performs co-monitoring when...
and institutions. They provide information on research developments, and new concepts in medical treatment. The Medical Science Liaison will also participate in close partnership with Site Management & Monitoring staff in the initiation, oversight, and follow-up of...
local/international regulations, including data protection legislation.
Conduct feasibility, site selection, initiation, monitoring, and close-out visits at investigational sites.
Collaborate with Regulatory Affairs and Clinical Operations teams on study...
affecting workplace health and ensure compliance with Amazon’s policies as well as all local health, safety, and medical regulations.
• Define, monitor, and report health‑related metrics to Workplace Health & Safety (WHS) Global Medical and Health (GMH)...
managed APIs and biomedical/clinical models (e.g., BioBERT, PubMedBERT, MedGemma, Meditron, and similar), and assessing where they may be appropriate for internal research support in line with technical, governance, and compliance considerations...
Review, approve, and ensure completeness and accuracy of batch manufacturing records, supporting the Qualified Person (QP) in the timely release of Phase I/II clinical trial radiopharmaceutical products.
• Ensure timely collection, monitoring...
ER Services Sagl ER Services Sagl is seeking a Product Specialist on behalf of its client, a company specialized in Clinical Laboratory Information Systems, based in Ticino. The selected candidate will develop in-depth knowledge of the company's...