Clinical Study Coordinator — GLP & Scheduling

Labcorp; Huntingdon; On-site; GBP 28,000 - 36,000; Full time

Job summary

Labcorp in the United Kingdom is seeking a Study Coordinator to join the site in Alconbury, Cambridgeshire. The role supports routine and non-routine toxicology studies, coordinating protocols, costing and scheduling in accordance with GLP and regulatory guidelines.

You will monitor in-life progress, interact professionally with clients, and provide administrative backup to Study Directors while developing project management skills.

Qualifications

• Knowledge of GLPs and regulatory guidelines.
• Strong attention to detail and accuracy.
• Good communication and responsiveness with teams and clients.
• Basic scientific understanding of industry requirements.

Responsibilities

• Coordinate routine and non-routine studies in compliance with company standards, GLP and regulations.
• Provide administrative support for toxicology studies including protocol development, costing and scheduling.
• Monitor in-life progress and interact professionally with clients.
• Draft protocols and amendments for Study Director review and approval.
• Take and distribute meeting minutes and support pre-initiation/related meetings.

Skills

GLP knowledge

Attention to detail

Communication skills

Scientific knowledge

Education

GCSE or equivalent

Job description

Labcorp in the United Kingdom is seeking a Study Coordinator to join the site in Alconbury, Cambridgeshire. The role supports routine and non-routine toxicology studies, coordinating protocols, costing and scheduling in accordance with GLP and regulatory guidelines.

You will monitor in-life progress, interact professionally with clients, and provide administrative backup to Study Directors while developing project management skills.