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Posted: 02-Oct-25
Location: Harrogate, United Kingdom
Type: Full-time
Categories:
Internal Number: 2533224
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
We can offer you:
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
Education / Qualifications:
BSc, preferably Life Science degree. Experience may be substituted for education
Skills / Experience:
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
Study Coordinators in toxicology are exposed to many different types of study and have the opportunity interact with all departments involved in pre-clinical toxicology studies in Harrogate 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. If this sounds like the role for you, then apply today!
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.
We encourage all to apply
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