Perform the duties of a Study Director/Principal Investigator for studies allocated by Management
Ensure that Study Plans conform with the intentions of the study design agreed with the Sponsor is prepared, signed and circulated and all standard test methods meet the current requirements of specific regulatory or test guidelines
Ensure that the agreed timelines are consistent with the Sponsors needs and/or agreed company start up times. Hold study start-up meetings, to ensure all key staff are conversant with all aspects of the study and to resolve any issues before treatment is started, to prevent unnecessary use of animals where applicable
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. To 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 compliant with Good Laboratory Practice 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. Make interim decisions regarding necessary amendments, to document such changes and to agree them with the Study Sponsor. 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
Inform the Sponsor of the results as soon as possible after the study completion date. Prepare draft and final reports ensuring the report is concisely and accurately written, reflects the raw data and includes all relevant information
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
Maintain computerised monitoring system for studies such that the information is up to date to enable study monitoring by their supervisors and other departments
Communicate with Ecotoxicology in the conduct of studies
Co-ordinate the supply of test vessels and equipment in conjunction with other members of staff thereby ensuring their availability for study start up
Contribute to the general management of the Analytical department in areas outside of that required as a Study Director
Travel as necessary, or to be available in-house to meet current and prospective sponsors to discuss existing and future studies
Keep up-to-date with trends in relevant analytical areas. Review specific topics as necessary so as to be able to discuss with Sponsors
Assist in the training, supervision and mentoring of technical staff and trainee Study Directors
Provide advice and support to internal and external customers relating to any study and non-study related topics
Perform those duties of other members of staff absent due to sickness, holidays or training. Overtime may be required in response to work-load demands., We are looking for a Study Director is to ensure that studies are conducted to agreed schedules by liaising with key staff involved in study conduct and maintaining an awareness of all aspects of the studies ensuring that a Study Plan is prepared, approved and implemented. Informing the Sponsor of study progress and preparing study reports that accurately reflect the raw data obtained. Ensuring suitable levels of compliance of all laboratory data, documentation and procedures conducted within the department and satisfy the requirements of GLP and Company SOPs and provide advice and support to internal and external customers relating to study designs and regulatory issues, as required.

Degree in Chemistry
Significant experience within a Study Director role in Analytical Chemistry
Knowledge of GLP and regulatory guidelines
Knowledge of data interpretation and report writing for studies
Experience of customer service communication
Proficiency in project management skills
Ability to conduct literature review
Due to the remote location of this site, there are no public transport links available

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.

Competitive salaries
No weekend work
Wider benefits package including pension and generous holiday allowance

2 contract Biotechnology / Life Sciences jobs in Peterborough