Study Coordinator - Toxicology

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Job description

* 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 Huntingdon we are looking to recruit a Study Coordinator to join the team. *

* Labcorp Drug Development is a global, world-leading Life Sciences Contract Research Organisation 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 offers flexible working with the opportunity for some remote working and is an excellent option for those that already have experiencein a similar role or within the pre clinical toxicology arena looking for progression.

* The Study Coordinator: *

* Provides scientific and administrative support to the Study Director for assigned toxicology studies from award, through the in-life phase. This involves multiple study set up tasks including protocol development, scheduling and initiation meetings
* Proactively liaises with clients, study monitors, Principal Investigators and internal departments to ensure accurate and timely protocol and amendment development and distribution
* Works with key clients and learns to implement action plans for solving study problems as they occur, including participation in client issue resolution process and any associated internal or external discussion
* Co-hosts or independently hosts client visits. May also assist with regulatory visits as appropriate
* Possesses the ability to mentor and train less experienced staff members

* 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 contributorypension
* 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
* Flexible working
Education/Qualifications:
* BSc, preferably Life Science degree. Experience may be substituted for education
Experience:
* Significant demonstrable experience in Toxicology or Study Coordination
* Demonstrates 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