Report Co-ordinator - In-vitro Genetic Toxicology

The Study Coordinator is responsible for coordinating the activities of Genetic Toxicology studies and you will work alongside the Study Directors, providing scientific and administrative support in the conduct and organization of multiple studies and study types. Please note, this is an office based role.,

• Provide support for Study Directors on day-to-day study specific tasks
• Coordinate packages of studies
• Draft protocols and amendments for Study Director review and approval
• Initiate scheduling requests and request changes to schedules
• Take responsibility for general study coordination tasks including scheduling shipping of samples, acquisition of test article and relevant documentation, sorting orders for studies and preparing documents for review e.g. solubility assessments and dose requests
  
  Do you have scientific knowledge in Genetic Toxicology paired with project management skills?, Bachelor's degree or equivalent experience, Experience with in vitro genetic toxicology and GLP knowledge and/or experience desirable
• Ability to write and prepare routine and complex study procedures, tables and graphs for reports
• Experience in technical writing, document production/publishing, and/or science preferred
• Demonstrates excellent communication, time management and organisational skills with the ability to manage multiple studies
• Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities
  
  Exposure to new and novel procedures with excellent career development opportunities in a supportive, growing team
• Competitive salaries and a comprehensive benefits package including health cover and contributory pension
• Opportunity for flexible and/or remote working after training