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Labcorp is seeking a Remote, UK based, Associate Document Coordinator to join our Pharmacokinetics/Toxicokinetics (PK/TK) team. Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. Work Schedule: Monday - Friday, 37 hours per week. As an Associate Document Coordinator, your primary responsibility will be the archiving of UK PK/TK data. This will involve tracking, preparing and compiling all required forms and data, working to study deadlines and communicating with various stakeholders. We are seeking motivated, career minded individuals who are interested in building a career with Labcorp and the PK/TK team. If you want to be a part of making a difference whilst also having the opportunity to work, learn and progress in a varied and supportive role, then apply today!
Job Responsibility
Works with Study Coordinators (SCs) and Analytical Coordinators (ACs), as appropriate, to prepare, monitor, maintain, and understand the finalization/archival scheduling mechanism and successfully performs applicable tasks around study archival
Notifies necessary personnel of study finalization/archival
Assists in gathering required paper/electronic items for archival
Prepares and proofs required paperwork in a timely, efficient, and error-free manner
Learns to read and understand study protocols, sample analysis outlines, amendments, study schedules, regulatory requirements, and Labcorp SOPs/P&Ps as they pertain to client deliverables (i.e. shipping, archival, data retrieval, and compilation etc.)
Learns to prepare and proof required paperwork for document and/or supply shipments in a timely, efficient, and error-free manner
Learns client-specific requirements for cover letters, inventories, or additional materials, as appropriate
Learns to proof tables and figures prepared by others
Learns and successfully performs applicable tasks around table and figure preparation, including proficiency with applicable data collection systems and preparation software
Learns and successfully performs report to data QC of at least one study type
Schedules study phases in coordination with the Study Director / Principal Investigator and lab operations
Requirements
Bachelor's degree in Life Sciences
Strong communication, organisation and time management skills
Excellent attention to detail
Ability to work collaboratively paired with a solution orientated approach
Ability to learn / utilise word processing software, database, spreadsheet, and specialised software