Regional Study Coordinator - Central Labs Services - Clinical Research

Labcorp•Indianapolis, IN

12d•$60,000 - $65,000•Hybrid

About The Position

Labcorp is seeking a hybrid Regional Study Coordinator to join our Central Labs Services team in Indianapolis. This role acts as a regional liaison between Global Study Managers and various CCLS departments, as well as between assigned Client representatives and the local CCLS platform. The Regional Study Coordinator will collaborate closely with the Global Study Manager on all study-related aspects throughout all study stages, from set-up to closure. This includes reviewing the study Statement of Work (SOW) for local feasibility, ensuring a detailed understanding of SOW specifications and their operational impact, managing day-to-day local study activities (logistics, monitoring, study supplies), and resolving local study issues. The role involves regular internal interaction and occasional external client interaction.

Requirements

High school diploma or equivalent
Two or more years of professional experience in a scientific or laboratory setting

Nice To Haves

Bachelor’s degree in a life science discipline
Proven ability to plan, prioritize, and manage workload in a fast‑paced environment
Strong communication and organizational skills
Excellent attention to detail with a collaborative, team‑oriented mindset
Demonstrated experience facilitating meetings and engaging effectively with clients

Responsibilities

Act as regional liaison between Global Study Manager and various CCLS departments involved in the study.
Act as regional liaison between assigned Client representatives (e.g., CRA, Site Monitors) and the corresponding local CCLS platform.
Occasionally represent Global Study Manager in interactions with the main client contact.
Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure.
Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead.
Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial.
Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development.
Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop.