At Labcorp we are committed to developing ourselves and our teams. We aim to create an environment that stimulates growth where you can achieve your fullest potential. This role is ideal for an aspiring life science graduate/professional looking for career development within a non lab based role.
This is an exciting opportunity for you to work as a Reporting Coordinator. In this role you will be working closely with Study Directors managing the full cycle of reporting. You will be working on many different animal studies and pulling/reporting the data.
The ideal candidate will have a science degree, as you will be needing to understand and translate the data you are working. Studies will be related to different animal studies. You will also be computer literate as you will be working on many different in-house systems.
Full training is provided and this is a hybrid role (home based, with occasion on-site Huntingdon visits).
The Reporting Associates I learns and performs the duties of drafting and finalizing nonclinical study reports and completes the following duties with limited supervision.
• General Duties
o Learns to and conducts contact with clients.
Prepares form letters and communication text.
Assists other client-facing staff (e.g., study director) with organizing client site visits and client conference calls
o Learns to and uses software tools to efficiently and accurately complete job duties. Types of software include word processing, spreadsheet, table generation, collaboration/sharing, and database applications.
o After completion of sufficient training, manages a full study workload with complex study designs by adhering to report preparation schedules and prioritizing tasks. Identifies and resolves changes to established study schedules to ensure client deliverables are met.
o After completion of sufficient training, begins to learn leadership within the reporting solutions group on activities such as performing peer reviews, preparing and delivering presentations, participating in staff meetings, participating in process improvement projects, and/or liaising with cross-site staff.
o After completion of sufficient training, may provide training and mentoring to new reporting associate staff members.
• Report Preparation
o Learns to and prepares the study report using details described in the protocol, protocol amendments, and study communications and Covance or client-specific requirements
o Learns to and incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
o Learns to and prints, binds, and mails draft and final study documents
o Learns to and addresses quality assurance inspection items on GLP-regulated studies
o Learns to and finalizes study reports and obtain, prepare, and deliver materials to archives
o Learns to and prepares report amendments
o Learns to and assists in the preparation of tabulated summaries in association with the study director
• Data Table Preparation
o Learns to and prepares data tables including completing basic statistical analysis in table generation programs.
o Learns to and drafts and quality checks data tables that were manually prepared
o Learns to and reviews data tables for accuracy
• Scheduling Responsibilities
o Learns to and reviews and adjusts the reporting schedule to ensure client expectations are met
o Learns to and schedules and leads the prewriting meeting, as required
o Learns to and schedules and coordinates study report finalization efforts
o Learns to coordinate expedited reporting, as necessary, among global counterparts
Science degree or relevant experience
Strong attention to detail
Labcorp is proud to be an Equal Opportunity Employer:
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