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Are you looking for a career change or to further your skill development in a rapidly growing area of the BiopharmCMC business?
Would you like to work for a leading global life sciences company, supporting an operational team, making a real impact to people’s lives with your work?
Our site in Harrogate is currently recruiting for a Study Coordinator to join our Molecular BioA team in a full-time, permanent role.
You will be a part of the larger lab function, aiding important work that is integral to our mission to improve health and improve lives!
Primarily your role with involve supporting our Senior Scientists with their day-day activities, drafting protocols, liaising with clients, handling/processing data and drafting reports.
Full training will be provided and is an ideal role for someone who has an interest in science but doesn’t want to work in a lab.
Job responsibilities include
- Writes Study Protocols, Methods and Report
- Drafts protocols, methods, amendments, and reports; utilizing sources such as Documentum, Toxicology protocols and client supplied information
- Reviews study activities for compliance against protocol/SOW, Standard Operating Procedure (SOP), Policies, and regulatory agency guidelines.
- Assists Lead Scientist with report preparation, including table and figure preparation; compiles analytical information from operations teams.
- Supports with Quality Assurance Unit (QAU) audits of study documents, drafts responses as applicable
- Supports report production processes through finalization
- Assists with archiving of study related materials
- Drives/Maintains Study and Client Communications
- Efficiently communicate and serve as a secondary to support the Lead Scientist with client contact on assigned studies.
- Proactively communicates and interacts with study team, other departments, and clients
- Attends and engages in pre-initiation and other internal study-related meetings, and attends conference calls; takes and distributes meeting minutes / action items, as appropriate.
- Support PM’s and Lead Scientists with preparing for and attends routine client visits.
- Assists in the development and maintenance of standard protocol, method and Sample Analysis Plan (SAP) formats as needed.
- Study/Timeline Management
- Plans, prioritizes, and manages own workload and multiple responsibilities.
- Manages standard projects and study designs
- Maintains well-documented, organized, and up-to-date study files, including real-time study schedule updates, as applicable.
- Demonstrates active engagement with study progress/timelines.
About you
The successful candidate will be educated to Bachelor of Science (BS) degree in science or related field; experience may be substituted for education.
What Labcorp Drug Development can offer you
- Competitive salaries
- Excellent benefits package
- Industry-leading training with the opportunity to build a long-term career
Experience
- Excellent attention to detail and can work to strict deadlines
- Experience of administration work
- Computing skills, including word processing and use of spreadsheets (e.g. Microsoft Office packages and Microsoft Project)
- General management and interpersonal skills to participate in a positive culture and collaboration within internal teams
- Good communication skills to be able to communicate effectively at all levels internally as well as with external clients, suppliers, etc.
- Ability to learn/utilize word processing software, database, spreadsheet, and specialized software
- Ability to prioritize, organize, and manage time
Labcorp is proud to be an Equal Opportunity Employer:
