Study Director - Physical Chemical Testing

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Labcorp is seeking a Study Director to join our team at Eye, Suffolk. Work Schedule: Monday - Friday – 37.5hrs Job Responsibilities: Act as GLP (Good Laboratory Practice) Study Director for studies to which they are appointed by management in accordance with the requirements of UK Statutory Instrument 1999 No. 3106 The Good Laboratory Practice Regulations 1999, including subsequent amendments and in line with OECD GLP expectations To perform the duties of a Study Director/Principal Investigator for studies allocated by Management and ensure that a Study Plan conforming with the intentions of the study design agreed with the Sponsor is prepared, signed and circulated Ensure all standard test methods meet the current requirements of specific regulatory or test guidelines and  ensure that the agreed timelines are consistent with the Sponsors needs and/or agreed company start up times Ensure that test and control items have been suitably tested for identity, stability etc. and that all necessary technical data regarding known toxicity, hazards of the test item or related materials have been obtained from literature searches and ensure that technical staff are aware of known hazards relating to a particular test item Monitor the status of observations made during the study and ensure the responses are fully documented.  Maintain an overview of the implication of these observations Review all data to ensure its accuracy and that checking procedures have been observed.  To ensure that the study is compliant with GLP and that suitable responses/actions are made following Quality Assurance Audit Be aware of the study status, anticipate problems that may affect the schedule date, purpose or integrity of the study.  To make interim decisions regarding necessary amendments, to document such changes and to agree them with the Study Sponsor.  To communicate with the Sponsor and Departmental and Project Management as required with particular regard to problem areas which may affect completion date or content of the study. To inform the Sponsor of the results as soon as possible after the study completion date.  To prepare draft and final reports ensuring the report is concisely and accurately written, reflects the raw data and includes all relevant information To transfer all study data and reports to the Archive in a timely manner following the issue of the final report, in accordance with Company procedures and SOPs To plan on a weekly basis schedules for allocated studies, ensuring that the earliest possible start date, consistent with the Sponsor's needs or agreed company start up and inform the appropriate manager of any proposed alteration in the planned schedule Maintain the computerised monitoring system for studies such that the information is up to date to enable study monitoring by their supervisors and other departments such as Quality Assurance Where appropriate co-ordinating the supply of test vessels and equipment in conjunction with other members of staff thereby ensuring their availability for study start up To maintain close verbal