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...
Responsible formanagement 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...
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...
sampling, and clinical observations
• Monitor outsourced preclinical studies at CROs to ensure quality and compliance
• Develop new experimental methods and coordinate inter-laboratory activities
• Draft operational procedures and SOPs
• Support technical...
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...
and clinical observations, while conducting diagnostic and instrumental evaluations. Your responsibilities extend to monitoring outsourced preclinical studies at CROs to ensure quality and compliance. You will develop new experimental methods, coordinate inter...
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...
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)...
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...
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...
materials (e.g., Study Monitoring Plan, Data Management Plans, CRFs, site training materials, Advertising Materials, etc.) as required.
• Oversee the work of CROs and other vendors (Central Labs, Clinical Supply Distributors, etc.) as assigned to clinical...
involved.
About the Role
As an Application Analyst, you will be the trusted expert supporting healthcare organizations in implementing InterSystems solutions effectively and efficiently. Your deep understanding of business processes, clinical workflows...