Ecotoxicology Study Director | GLP Expert

. Labcorp Early Development Laboratories Limited; Huntingdon; Presencial; GBP 65.000 - 85.000; Tempo integral

Benefícios oferecidos por esta vaga

Competitive salary

No weekend work

Pension and generous holiday allowance

Resumo da vaga

Labcorp Early Development Laboratories Limited is seeking a Study Director - Ecotoxicology for our Alconbury site near Huntingdon, Cambridgeshire. The role focuses on leading ecotoxicology studies, ensuring GLP compliance, and coordinating with sponsors and staff to achieve timely, quality results.

Key duties include study design conformity, staff briefings, data interpretation, report writing, and regulatory adherence.

Qualificações

• Degree in Environmental Sciences or Ecotoxicology.
• Significant experience as Study Director in Ecotoxicology.
• Working knowledge of GLP and regulatory guidelines.
• Skilled in data interpretation and report writing for studies.
• Skilled in customer service communication.
• Proficiency in project management.
• Ability to conduct literature review.

Responsabilidades

• Perform the duties of a Study Director/Principal Investigator for ecotoxicology studies following guidelines.
• Ensure Study Plan conforms with study design and guidelines.
• Lead start-up meetings and coordinate staff.
• Verify test items and hazards information.
• Ensure regulatory compliance and GLP.
• Monitor observations and document results.
• Prepare and finalize study reports with raw data.
• Archive study data and reports per SOPs.

Conhecimentos

Study Director experience in Ecotoxic2

GLP knowledge

Data interpretation

Customer service communication

Project management

Literature review

Formação

Degree in Environmental Sciences or Ecotoxicology

Descrição da vaga

Labcorp Early Development Laboratories Limited is seeking a Study Director - Ecotoxicology for our Alconbury site near Huntingdon, Cambridgeshire. The role focuses on leading ecotoxicology studies, ensuring GLP compliance, and coordinating with sponsors and staff to achieve timely, quality results.

Key duties include study design conformity, staff briefings, data interpretation, report writing, and regulatory adherence.