valuta e seleziona, in collaborazione con il Clinical R&D Manager, con il Clinical Operation Lead ed il Clinical Scientist, i centri sperimentali ed eventuali terze parti, da utilizzare negli studi clinici.
6. Monitora periodicamente il budget di studio...
regulatory requirements.
RESPONSIBILITIES:
• Lead the planning, implementation, and execution of clinical trials, ensuring adherence to
timelines, budget, and quality standards.
• Oversee site selection, recruitment, and monitoring activities for clinical...
Job Overview
Engage in structured training program to gain knowledge and skills required to independently conduct clinicalmonitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable...
The Junior Statistical SAS Programmer, under the supervision of the Direct Manager, is mainly involved in developing SAS programs for the generation of datasets, tables, figures and listings for clinical studies (according to ICH E3), publications...
Job Summary
Our clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our ClinicalMonitoring team in Italy. This position will work with a team to accomplish...
Plan [DMP], Prescription Drug Monitoring Program [PDMP], Case Report Form [CRF], Clinical Study Report [CSR])
• Provide high-quality and timely statistical analyses results to support correct and timely decision making.
• Act as a statistical...
Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:
Business...
regulatory requirements.
RESPONSIBILITIES:
• Lead the planning, implementation, and execution of clinical trials, ensuring adherence to
timelines, budget, and quality standards.
• Oversee site selection, recruitment, and monitoring activities for clinical...
start-up activities including Engineering Runs, GMP/clinical, PPQ and routine commercial runs, and resulting risk mitigation activities.
• Process Validation and Continued Process Verification activities.
• Offers molecule steward and drive process...
Clinical Research Associate, Sponsor Dedicated - Italy
Clinical Research Associate, Sponsor Dedicated - Italy
Apply locations Milan, Italy time type Full time posted on Posted 2 Days Ago job requisition id R1476107
Experienced Clinical Research...
Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:Business...
Functions:
1. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization...
Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:
Business...
gathering and analyzing market data, industry trends, and internal performance metrics to inform the Company’s strategy; - Assist in defining and monitoring short-term KPIs aligned with the Strategic Plan, helping coordinating input at cross-functional level...
About Accelera
Accelera is a Preclinical CRO (Contract Research Organization) and offers unparalleled expertise in bringing innovative drug candidates from the Discovery to the Clinical Phases.
Over the years, Accelera has brought new products...