Clinical Monitoring and Site Management Expert

Clinical Research Associate RoleThis is a role that involves conducting on-site and remote monitoring of clinical research studies. The primary objective is to ensure quality monitoring through the development of tools, procedures, and processes.Key Responsibilities:Performs site qualification, site initiation, interim monitoring, site management activities...

We are seeking a Senior Clinical Research Associate to join our team.As a Senior Clinical Research Associate, you will be responsible for monitoring clinical trials in oncology. The ideal candidate will have at least 1.5 years of on-site monitoring experience and a strong understanding of Good Clinical Practice.You will work closely with sites to adapt,...

Clinical Research Associate II / SR.CRA (Level depends on experience)1 week ago Be among the first 25 applicantsAbout CTICTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations.We assist...

Senior Clinical Research Associate RoleAt the forefront of clinical development, we're seeking an accomplished Senior Clinical Research Associate to spearhead the oversight and management of clinical trial activities. This role demands meticulous attention to protocol, regulatory requirements, and industry standards, ensuring seamless execution throughout...

Clinical Site Navigator RoleDeliver exceptional site management and regulatory compliance as a Clinical Site Navigator.This hybrid role combines start-up and iHCRA/CRA responsibilities to ensure seamless progression from feasibility to site activation, through maintenance phase as required.Coordinate site-level activities throughout the start-up phase of a...

Oncology Clinical Monitoring Associate We are seeking an experienced and motivated professional to join our global clinical team as a Clinical Monitoring Associate. This role will be responsible for ensuring the integrity of clinical trials by conducting site visits, monitoring data quality, and maintaining relationships with key site personnel.Key...

Job DescriptionClinical trials rely heavily on the expertise of Clinical Research Associates. As a CRA II, you will be responsible for upholding the integrity and quality of clinical trial data.Key Responsibilities:Develop project plans related to Clinical Monitoring responsibilities.Ensure informed consent procedures and protocol requirements are adhered...

Job OverviewWe are seeking a skilled professional to conduct site initiation visits and monitor clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.Main Responsibilities:Conduct site initiation visits and monitor clinical trials to ensure adherence to regulatory standards.Coordinate data collection,...

Clinical Research Associate Role Summary:Fortrea is seeking a skilled Clinical Research Associate II to oversee site management for clinical studies and conduct site monitoring responsibilities.The ideal candidate will have thorough knowledge of ICH GCP Guidelines, a strong understanding of local regulatory requirements, and excellent communication...

Senior Site Manager Job PostThe Senior Site Manager is responsible for ensuring inspection readiness through compliance with clinical trial protocols, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations.Key Responsibilities:Act as primary contact for assigned sites for specific trials.Participate in site...