Perform site initiation, routine monitoring, and close-out visits. Review and verify case report forms (CRFs) against source documents. Identify and resolve data discrepancies. Ensure proper documentation and timely repo...

We are looking out for a Sr. Clinical Research professional who has a relevant experience and has excellent knowledge. Beacon Targeted Therapies ( https: / / beacon-intelligence.com / ) Beacon provides a customi...

Job descriptionShould have knowledge in clinical research studies Perform Site visits (i.e. Site Selection Visit, Site Initiation Visits, Site monitoring visits and site close-out visits)should have knowledge in ICH GCP Guide...

Job descriptionShould have knowledge in clinical research studies Perform Site visits (i.e. Site Selection Visit, Site Initiation Visits, Site monitoring visits and site close-out visits)should have knowledge in ICH GCP Guide...

You'll typically be involved in all stages of the clinical trial, including identifying an investigational site and setting up, initiating, monitoring and closing down the trial. Clinical Research Associate Responsibilities:...

Job Summary We are seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and ...

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track subject recruitme...

You will be required to manage the data collected during trials, oversee trial sites, and conduct regular site visits to monitor the progress. You will also collaborate with the sponsors at trial sites and ensure the tests ar...

Responsibilities:Detailed Duties: List of specific responsibilities, including: Conducting site initiation, monitoring, and close-out visits. Ensuring compliance with GCP, ICH guidelines, and regulatory requirements. ...