Clinical Site Associate Oncohematology | C-067

.766 million patients were reached with Novartis medicines. We aspire to get Novartis medicines in the hands and homes of patients by delivering a Triple Win: A Win for Patients; A Win for Healthcare Systems, and A Win for Novartis.- The Clinical Site Associate performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Oncology and Hematology clinical trials within the country. The Clinical Site Associate is responsible to deliver data within timelines and required quality standard, and for adherence to monitoring procedures in accordance with GCP and ICH, local regulations and SOPs.-**Your responsibilities include,but are not limited to**:- Trial Monitoring strategy- Conducts feasibility and screen potential Investigators and networks to evaluate capabilities for conducting clinical trials Allocation, initiation and conduct of trials- Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial- Is the frontline liaison between Novartis and sites to ensure successful collaboration, meeting Novartis expectation on milestone and deliveries- Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and Novartis procedures- Facilitates the preparation and collection of site and country level documents- Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Retrains site personnel as appropriate- Conducts continuous monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, GCP,global and local regulations, global and local processes to secure data integrity and patient safety- Is accountable for continuously updating all electronic systems (global and local) relevant to perform job functions- Ensures that study milestones for sites responsible are met as planned (i.E., study startup, recruitment, database analyses, closeout, etc