Are you proactive, enjoy working with people and have a keen interest in toxicology?
Are you looking to take the next step in your career?
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:
* Provides administrative and scientific support for toxicology studies, including pre-study tasks (e.g., protocol development, costing, scheduling), monitoring the in-life progress of assigned studies, and interacting with clients.
* Provides administrative backup support for Study Directors on day to day study-specific activities or tasks.
* Learns to ensure study compliance with the protocol, standard operating procedures, Good Laboratory Practices, and other regulatory guidelines.
* Learns to plan, prioritize, and manage a workload and the associated responsibilities.
* Serves as a contact, along with the Study Director, in communication and interactions with other departments and clients, with assistance as applicable.
* Learns to draft protocols and amendments for Study Director review and approval.
* Ensures all client comments on protocols and amendments are addressed in a timely manner.
* Schedules and participates in pre-initiation and other study-related meetings, as required, and takes and distributes pre-initiation meeting minutes.
* Learns to draft and submit appropriate documents to the IACUC/AWERB for approval.
* Learns to address and review 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.
* Assists with hosting client visits.
* Assists Study Director by ensuring that study documentation such as Literature Reviews and Animal Order Forms are in place.
* Prepares shipping documentation including CITES application requests and any other associated shipping documentation, as required per study.
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:
* Some experience or knowledge in Toxicology/Study Coordination or a client facing position.
* 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.
If this sounds like the role for you, then apply today!
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