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Labcorp is seeking a Study Director – Analytical Chemistry to join our Environmental/Ecotoxicology team at Alconbury, near Huntingdon, Cambridgeshire
Work Schedule: Monday - Friday – 37.5 hrs
Job Responsibilities:
- 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.
Minimum Qualifications:
Additional Job Standards:
- 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
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.
Benefits:
- Competitive salaries
- No weekend work
- Wider benefits package including pension and generous holiday allowance
If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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