Report Coordinator - In-vitro Genetic Toxicology

Laboratory Corporation; Harrogate; On-site; GBP 25,000 - 35,000; Full time

Job summary

Labcorp is seeking a Study Coordinator for their Genetic In-Vitro Toxicology department in Harrogate. This role involves coordinating study activities, supporting Study Directors, and managing multiple studies. Ideal candidates possess a Bachelor's degree and have experience in genetic toxicology, with strong organizational and communication skills. The position offers career development opportunities and a comprehensive benefits package.

Benefits

Competitive salaries

Comprehensive benefits package including health cover and pension

Opportunity for flexible and/or remote working after training

Qualifications

• Experience with in vitro genetic toxicology and GLP knowledge desirable.
• Ability to write and prepare study procedures, tables, and graphs.
• Experience in technical writing and document production preferred.

Responsibilities

• Coordinate activities of Genetic Toxicology studies.
• Provide support for Study Directors on day-to-day tasks.
• Initiate scheduling requests and manage study coordination tasks.

Skills

Attention to detail

Time management

Organizational skills

Communication

Technical writing

Education

Bachelor’s degree or equivalent experience

Job description

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 a 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 contributorypension

• 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

• Flexible hours considered

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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