Band 4 Clinical Research Assistant London, England
Job description
The Royal Free Hospital actively participates in a diverse range of clinical research sponsored both academically and commercially. We are currently seeking a motivated and enthusiastic Clinical Research Assistant to join our welcoming research team. The successful applicant will assist in the provision of the clinical trial service to Vaccine Portfolio within the Vaccine Research team which is based at Royal Free Hospital.
The role of the Clinical Research Assistant is to provide patient centred care and administrative support to the research team. The post holder will provide support to research nurses/practitioners, medical staff, and data manager, aiding in the collection and processing of clinical trial data for our current range of clinical trials in the Vaccine Portfolio.
Responsibilities will include performing observations, assisting in identifying and recruiting participants to clinical trials, managing sample collection including phlebotomy and processing of clinical trial samples, creating and maintaining Investigator site files and supporting basic trial administration.
The post holder will be expected to develop skills and knowledge relating to the conduct of clinical trials and specialist area of practice. The post holder will demonstrate clinical data processing and management in accordance with Standard Operating Procedures (SOPs) and ICH - Good Clinical Practice (GCP) at all times.
The post holder will offer World Class Care to service users, staff, colleagues, clients and patients alike.
The role of the Clinical Research Assistant is to provide patient centred care and administrative support to the research team. The post holder will provide support to research nurses/practitioners, medical staff, and data manager, aiding in the collection and processing of clinical trial data for our current range of clinical trials in the Vaccine Portfolio.
Responsibilities will include performing observations, assisting in identifying and recruiting participants to clinical trials, managing sample collection including phlebotomy and processing of clinical trial samples, creating and maintaining Investigator site files and supporting basic trial administration.
The post holder will be expected to develop skills and knowledge relating to the conduct of clinical trials and specialist area of practice. The post holder will demonstrate clinical data processing and management in accordance with Standard Operating Procedures (SOPs) and ICH - Good Clinical Practice (GCP) at all times.
