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...

A Clinical Research Analyst is responsible for collecting, analyzing, and reporting on clinical data to support research studies and trials. They work closely with researchers, doctors, and other healthcare professionals to e...

An organisation is searching for an Associate Director within Clinical Research Lead, please see some of their job details below. Clinical Investigator Management Accountable for activities required at clinical trial sites ...

The University of Southampton Faculty Of Medicine is offering an appointment to be based within the Southampton Clinical Trials Unit (SCTU) at Southampton General Hospital. This post holder will work within SCTU supporting t...

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Qualification &...

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Qualification &...

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. ...

World Cancer Research Fund Clinical Research Training Fellow in breast cancer This post offers the opportunity for a Doctor in specialist training to gain experience in breast cancer research within a comprehensive centre fo...

A Clinical Research Officer is responsible for overseeing the execution of clinical trials, ensuring they are conducted according to established protocols, regulatory guidelines, and ethical standards, by managing study sit...