Study Coordinator

4 weeks ago

Harrogate, North Yorkshire, United Kingdom Labcorp Full time

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 Harrogate, North Yorkshire, we are looking to recruit a Study Coordinator to join the team.

Labcorp Drug Development 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:

  • Provides administrative and scientific support for toxicology studies, including pre-study tasks (e.g., protocol development, costing, scheduling), monitoring the in-life progress of assigned studies, and interacting with clients
  • Provides administrative backup support for Study Directors on day to day study-specific activities or tasks
  • Learns to ensure study compliance with the protocol, standard operating procedures, Good Laboratory Practices, and other regulatory guidelines
  • Learns to plan, prioritize, and manage a workload and the associated responsibilities
  • Serves as a contact, along with the Study Director, in communication and interactions with other departments and clients, with assistance as applicable
  • Learns to draft protocols and amendments for Study Director Review and approval
  • Ensures all client comments on protocols and amendments are addressed in a timely manner
  • Schedules and participates in pre-initiation and other study-related meetings, as required, and takes and distributes preinitiation meeting minutes
  • Learns to draft and submit appropriate documents to the IACUC/AWERB for approval
  • Learns to address and review 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
  • Assists with hosting client visits
  • Assists Study Director by ensuring that study documentation such as Literature Reviews and Animal Order Forms are in place
  • Prepares shipping documentation including CITES application requests and any other associated shipping documentation, as required per study

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:

  • Some experience or knowledge in Toxicology/Study Coordination or a client facing position
  • 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:

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.

We encourage all to apply

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