Study Coordinator - Toxicology

Do you have fantastic organisational skills and want to work in the pharmaceutical industry supporting a growing Toxicology team?

Are you looking for a role with career progression opportunities?

Do you want to be a part of the world's leading drug development company?

At our site in Harrogate, North Yorkshire, we are looking to recruit a Study Coordinator to join the team.

Labcorp is a global, world-leading Life Sciences Contract Research Organization that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical, crop protection and chemical industries. We strive to make a difference to people's everyday lives by bringing essential medicines to the market.

The Study Coordinator is responsible for coordinating the activities of routine and non-routine toxicology studies, in compliance with the appropriate company standards, Home Office requirements and regulatory guidelines, in a timely, efficient manner.

This role is an office-based, on-site position however offers the possibility for flexible working after training.

The Study Coordinator:

• Is familiar with standard operating procedures, capabilities, and regulatory guidelines. Serves as a team resource for questions related to these topics.
• Provides leadership to study teams and successfully manages difficult projects
• May lead client or internal discussions, with input from Study Director, related to study design changes and study issues
• Serves as a contact, along with the Study Director, in communication and interactions with other departments and clients, with assistance as applicable
• Drafts protocols and amendments for Study Director Review and approval
• Ensures all client comments on protocols and amendments are addressed in a timely manner
• Addresses and reviews quality assurance audits relating to protocols and amendments and reports (as applicable), with oversight. Follows up with appropriate personnel to ensure all necessary document/data clarifications are completed in the specified timelines
• Identifies opportunities for process improvements and assists in their resolution. May participate in other process improvement teams
• Manages increasingly complex projects and study designs while taking on an increased workload
• Provides input and assist with implantation of new technology and system changes/upgrades/enhancements

• Exposure to a variety of studies and the opportunity to interact with all departments involved in pre-clinical toxicology studies from client managers to reporting teams. This enables opportunities to develop knowledge, progress within the team and potentially to wider roles in Safety Assessment in the future
• Competitive salaries and a comprehensive benefits package including health cover and contributory pension
• Unrivalled opportunities to develop a successful career in the scientific industry
• Unsurpassed career development opportunities where you can learn as you develop in a supported team environment
• A culture of CARE with access to well-being programs and various employee resource groups
• Flexible working

• BSc, preferably Life Science degree. Experience may be substituted for education

• Significant demonstrable experience in Toxicology/Study Coordination or a client facing position, preferably within a CRO
• Ability to demonstrate excellent communication and time management skills
• Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities
• Knowledge of GLPs, regulatory agency guidelines and Home Office requirements