Study Director - Analytical Chemistry - Environmental Ecotoxicology

. Labcorp Early Development Laboratories Limited; Huntingdon; Presencial; GBP 65.000 - 85.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Competitive salaries

No weekend work

Pension and generous holiday allowance

Descripción de la vacante

Labcorp is seeking a Study Director - Analytical Chemistry to join the Environmental/Ecotoxicology team at Alconbury, near Huntingdon, Cambridgeshire.

The role involves leading studies, ensuring GLP compliance, coordinating with sponsors, and delivering accurate reports. The position is on-site with regular Monday–Friday hours and opportunities for growth within a global laboratory services leader.

Formación

• Knowledge of GLP and regulatory guidelines.
• Ability to interpret study data and write reports.
• Experience coordinating projects and timelines.

Responsabilidades

• Perform the duties of a Study Director/Principal Investigator for studies allocated by Management.
• Ensure Study Plans conform with study design and are signed and circulated.
• Hold study start-up meetings to ensure staff are ready and issues are resolved promptly.
• Ensure test items are tested for identity and hazards; obtain technical data from literature.
• Monitor observations, verify data accuracy, and ensure QA compliance.
• Communicate with Sponsor and management about study progress and issues.
• Prepare draft and final reports reflecting raw data accurately.
• Transfer study data to the Archive following final report issuance.
• Maintain monitoring systems and coordinate with Ecotoxicology and other staff.
• Travel as necessary to meet sponsors and discuss studies.

Conocimientos

GLP knowledge

Data interpretation

Report writing

Project management

Customer service

Educación

Degree in Chemistry

Descripción del empleo

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 - 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 observationsReview 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 studyInform 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 informationTransfer 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 departmentsCommunicate 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 studiesKeep 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:

• Degree in Chemistry

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,

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. If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.