Study Coordinator - Dose Analysis

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

Are you looking for a role with training and career progression opportunities?

Do you have an interest in science but want to be office based?

Labcorp is a global, world-leading Life Sciences Contract Research Organisation 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 and products to the market.

We are currently seeking a Study Coordinator to join our Dose Analysis team in Harrogate, North Yorkshire.

• Serves as a contact with the Study Directors, in communication and interactions with other departments
• Proactively communicates and interacts with the Study Directors and Laboratory Operations to ensure key milestones are achieved
• Maintains well documented, organized and up-to-date study files
• Regularly update Dose Analysis Study Management and the Study Director on the status of assigned studies
• Perform checking of analytical data in a timely manner for assigned studies
• Prepare draft contributory reports/tables for assigned studies
• Identify and initiate Quality Events on the QMS (quality management system)
• Develop an understanding of the duties and role of a Study Director
• Report any difficulty, uncertainty or unexpected finding to Senior Dose Analysis personnel
• Assists in interpreting data for reports, prepares data and submits to QA (quality Audit)
• Co-ordinates return of study data to the Study Director/Sponsor after report finalisation.
• Performs archiving of study specific and non-study specific data. Ensuring all data is accounted for and tracked.
• Act as Document Controller for the department, prepares for new starter set up, including printing of material, portfolios and system/department access
• Prepares and performs administration for operational needs (e.g. Register of Signatures)
• Ordering of administrative material and provides administrative support/function for the department

• 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. With the support of exceptional people from across the globe and an energized purpose, you will be empowered to own your career journey with mentoring, training and personalised development planning
• The opportunity to work on a variety of studies
• Flexible working with the opportunity for some remote working upon completion of training

• "A" Level or equivalent, (Scientific or English degree is preferred.)
• OR relevant scientific industry experience

• Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
• Attention to detail, time management skills, and organizational skills
• Scheduling, tracking and logistic experience would be desirable
• Experience in technical writing, document production/publishing, and/or science desirable