Are you looking for a office based scientific role?

Do you have excellent communication skills and attention to detail?

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

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

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 ReportDrafts protocols, methods, amendments, and reports; utilizing sources such as Documentum, Toxicology protocols and client supplied informationReviews 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 applicableSupports report production processes through finalizationAssists with archiving of study related materialsDrives/Maintains Study and Client CommunicationsEfficiently 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 clientsAttends 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 ManagementPlans, prioritizes, and manages own workload and multiple responsibilities.Manages standard projects and study designsMaintains 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 salary and a comprehensive benefits package, including health coverage and contributory pension

Ability to work with a variety of different clients on wide ranging projects

Flexible working and career development opportunities

Industry-leading training with the opportunity to build a long-term career

Experience

Excellent attention to detail and can work to strict deadlinesExperience of administration workComputing 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 teamsGood 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 softwareAbility to prioritize, organize, and manage time

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

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