GLP Study Director – Chemistry Lead

Har Labcorp Early Development Laboratories Limited; Eye; Sur place; GBP 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

Competitive salaries

No weekend work

Pension and generous holiday allowance

Résumé du poste

Labcorp is seeking a Study Director to join the Eye, Suffolk team. You will oversee studies to GLP standards, prepare Study Plans, and ensure regulatory compliance with timelines.

The role involves coordinating data, reports, and QA processes while communicating with sponsors and internal teams. Bring degree-level chemistry and hands-on GLP experience, with proficiency in instrumental techniques (LC-MS/MS, GC-MS, HPLC-uv).

Qualifications

• Degree in Chemistry required.
• GLP study experience and ability to act as Study Director.
• Experience with LC-MS/MS, GC-MS or HPLC-uv instrumentation.
• Detail-oriented with the ability to manage multiple priorities.
• Willingness to travel as needed.
• Office-based role with strong written and verbal communication.

Responsabilités

• Act as GLP Study Director for assigned studies per regulations.
• Perform duties of Study Director/PI and prepare signed Study Plans.
• Ensure test methods meet regulatory requirements and timelines.
• Verify identity, stability and hazards of test items; obtain data.
• Monitor observations and document responses; inform sponsor.
• Review data for accuracy and GLP compliance with QA audits.
• Inform sponsor of results; draft and finalise study reports.
• Transfer data/reports to Archive per SOPs.
• Plan weekly study schedules and coordinate with management.
• Maintain monitoring system for studies; support QA and staff.
• Coordinate supply of vessels/equipment for study start-up.
• Maintain liaison with staff; adhere to policies and SOPs.

Connaissances

Attention to detail

Time management

Organisational skills

Quality assurance

Communication

Formation

Degree in Chemistry

Outils

LC-MS/MS

GC-MS

HPLC-uv

Description du poste

Labcorp is seeking a Study Director to join the Eye, Suffolk team. You will oversee studies to GLP standards, prepare Study Plans, and ensure regulatory compliance with timelines.

The role involves coordinating data, reports, and QA processes while communicating with sponsors and internal teams. Bring degree-level chemistry and hands-on GLP experience, with proficiency in instrumental techniques (LC-MS/MS, GC-MS, HPLC-uv).