Do you have fantastic organisational skills and want to work in the pharmaceutical industry supporting a growing Toxicology team?

Are you looking for a role with career progression opportunities?

Do you want to be a part of the world's leading drug development company?

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:

• Is familiar with standard operating procedures, capabilities, and regulatory guidelines. Serves as a team resource for questions related to these topics.

• Provides leadership to study teams and successfully manages difficult projects

• May lead client or internal discussions, with input from Study Director, related to study design changes and study issues

• Serves as a contact, along with the Study Director, in communication and interactions with other departments and clients, with assistance as applicable

• Drafts protocols and amendments for Study Director Review and approval

• Ensures all client comments on protocols and amendments are addressed in a timely manner

• Addresses and reviews 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

• Identifies opportunities for process improvements and assists in their resolution. May participate in other process improvement teams

• Manages increasingly complex projects and study designs while taking on an increased workload

• Provides input and assist with implantation of new technology and system changes/upgrades/enhancements

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:

• Significant demonstrable experience in Toxicology/Study Coordination or a client facing position, preferably within a CRO

• 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

Study Coordinators in toxicology are exposed to many different types of study and have the opportunity interact with all departments involved in pre-clinical toxicology studies in Harrogate 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. If this sounds like the role for you, then apply today!

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

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.

Logo

About Labcorp

Clear and confident health care decisions begin with questions. At Labcorp, we’re constantly in pursuit of answers. With unparalleled diagnostics and drug development capabilities, we accelerate innovation and provide insight to improve health and improve lives. Whether you’re a patient, provider, researcher or in the pharmaceutical industry, we’re here for you. More than 70,000 employees strong, we serve clients in more than 100 countries. Labcorp (NYSE: LH) reported revenue of $14 billion in FY 2020.

Connections working at Labcorp

More Jobs from This Employer

https://jobs.healthcareercenter.com/jobs/21715801/study-coordinator-toxicology