Total 3 science rd research job vacancies in Gillingham, ME5 5NY

The HSSW team report to the Biomedical Scientists who are responsible operationally for the Biochemistry Laboratory service. Duties include stock control of reagents, analyser maintenance, processing quality control samples and external quality assurance material. Working to standard operating procedures at all times. Performing manual testing procedures. Entering test results on to the laboratory information system Assisting with UKAS accreditation Dealing politely and effectively with phone calls,. Liaising with company engineers and other service users.

Will assist in the management of research projects providing the necessary support so that studies can be set up and conducted safely, efficiently according to the required standards & targets Assist in the delivery of recruitment targets in line with the contractual agreements, agreed time lines Open and manage allocated projects, set timescales and resolve problems. This includes management of the set up process Take responsibility for all areas of practice relating to the conduct of clinical trials and research studies Maintain accurate records of portfolio activities Under supervision, report, address, help to resolve any breaches and protocol deviations. Report Adverse Events (AEs) using appropriate procedures, including the expedited reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs) Prepare/assist with preparation of patient documentation for research-related treatment clinics, complete accurate records of patient care, maintain source data and Case Report Forms and all other trial documents in a manner conducive to audit

Will assist in the management of research projects providing the necessary support so that studies can be set up and conducted safely, efficiently according to the required standards & targets Assist in the delivery of recruitment targets in line with the contractual agreements, agreed time lines Open and manage allocated projects, set timescales and resolve problems. This includes management of the set up process Take responsibility for all areas of practice relating to the conduct of clinical trials and research studies Maintain accurate records of portfolio activities Under supervision, report, address, help to resolve any breaches and protocol deviations. Report Adverse Events (AEs) using appropriate procedures, including the expedited reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs) Prepare/assist with preparation of patient documentation for research-related treatment clinics, complete accurate records of patient care, maintain source data and Case Report Forms and all other trial documents in a manner conducive to audit