currently seeking a Clinical Contract Specialist office based in Italy.
Job Overview
• Prepare & negotiate site contracts for the assigned studies
• Monitor timelines for site contract and budget
• Point of contact for the Clinical Trial Agreements...
File) in collaboration with the Clinical Trial Administrator, ensuring the completeness and proper archiving of all study documentation.
• Budget Management:
• Monitor and reconcile study budgets, provide regular forecasts, and review invoices monthly...
independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality.
The CRA works closely with Lead CRAs, Sr...
in the e TMF and perform ongoing quality control of the e TMF (Investigational products and Clinical Trial Supply section) using Company System
• Monitor the e TMF quality issues and follow up with the relevant functions (internally / CMO /CRO) until...
Company Description
Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are...
country/cluster and supervises the monitoring, oversight activities of sites to ensure patient safety and quality of study execution in accordance with applicable prevailing laws, Good Clinical Practice, and Pfizer standards.
• Overall accountability for...
documentation is completed with appropriate strategies implemented.
• Support Residents and their families by addressing queries, comments, suggestions, or concerns.
• Manage, support, coach, monitor and mentor the clinical care team in the provision of quality...
Smart Dental Clinic, uno tra i più importanti network di centri odontoiatrici in Lombardia, facente parte del Gruppo San Donato, ricerca Clinic Coordinator da inserire in organico presso la sede IRCCS - Ospedale Galeazzi.
Nello specifico la risorsa...
independently all the activities related to the monitoring of clinical trials.
• Good knowledge of Office Suite (Word, Excel, PowerPoint).
• Organizational and problem-solving skills.
• Excellent written and verbal communication skills including a good command...
improvement, as required.
Education and Experience:
• University degree in a science related field
• CRA Qualified as per the Ministerial Decree dated 15/11/2011 and at least 1 year of independent monitoring experience in clinical development phases II-IV...
with clinical trial sites, serving as the Sponsor's primary point of contact between the organization and site personnel. The CRA remains the site's primary point of contact for all protocol and operational requirements.
• Monitor and analyze patient...
CPL TAYLOR by Synergos srl - Ricerca e Selezione Personale Qualificato-Verona
international
Company that operates within the Life Sciences industry & Technology field
and establishes itself as a long-standing partner for technology and expert
service providers across Clinical, Regulatory, Quality, Pharmacovigilance, and
Medical Affairs...
when applicable
• Develop operational project plans
• Manage risk assessment and execution
• Responsible for management of study vendor
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring...
and behavioral digital biomarkers. Together they enable the continuous remote monitoring of human health across a range of conditions, through clinical-quality digital measurements.
If you are looking to join a fast-paced growth environment and do meaningful...
Quality Assurance, Medical-marketing, Clinical Sciences, Pharmacovigilance), and local regulatory teams or external partners for the preparation of the regulatory application related to new registrations and lifecycle management
• Preparation of the master data...
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