New York, New York
New York, New York
Maple Grove, Minnesota
Summit, New Jersey
Nashville, Tennessee
Indianapolis, Indiana
Easton, Maryland
Posted: 28-Nov-24
Location: Harrogate, United Kingdom
Type: Full-time
Categories:
Internal Number: 2445809
Do you have scientific knowledge in Genetic Toxicology paired with project management skills?
Are you looking to work in an exciting new role where you can develop and grow to your full potential?
At our site in Harrogate, we are looking to recruit a Study Coordinator to join our Genetic In-Vitro Toxicology department within the Aerosol team.
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.
As Senior Study Coordinator you will:
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
What we can offer you:
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
Education:
Bachelor?s degree or equivalent experience
Skills / 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
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility.
For more information about how we collect and store your personal data, please see our Privacy Statement.