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Project Coordinator

Job in Johnson City, Washington County, Tennessee, 37603, USA
Listing for: LabConnect
Full Time position
Listed on 2025-12-22
Job specializations:
  • IT/Tech
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Join to apply for the Project Coordinator role at Lab Connect.

Overview

Lab Connect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.

We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor‑made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team and coordinating all laboratory related needs, advising on strategies for lab data collection and providing end‑to‑end analytical and logistical solutions.

Job Summary

The Project Coordinator is responsible for collaborating with the Project Managers, internal Lab Connect departments, sites, sponsors, with daily ongoing clinical trial study projects, requests, and specifications.

Please note: this is a fully remote role, ideal for candidates in EMEA who can support EU business hours.

Essential Duties and Responsibilities
  • Ensures appropriate communication channels are maintained with Sponsors and Contract Research Organizations as the Secondary Project Contact
  • Promptly responds to interactions with Project Managers, internal Lab Connect departments, sites, & sponsors.
  • Updates all on‑going project status to Project Managers as needed and monthly to direct manager.
  • Provides support for investigation and resolutions for Quarantine samples as needed.
  • Interfaces with, but not limited to, the following:
    Project Management, Sponsors, investigator sites, reference laboratories, Investigator Support Services, Clinical Trial Materials, Information Technology, Data Management personnel, and Executive Leadership Team.
  • Updates and maintains Study specific Site Lists containing vital site information that is utilized by multiple departments.
  • Verifies that Investigator’s Site information is accurate and up to date in all applicable databases.
  • Generates Lab Report Access Forms for anyone seeking access to Lab Reports
  • Receives, verifies, and processes all returned Lab Report Access Forms, including but not limited to: ensuring forms are filled out properly, filed on SharePoint in study specific folder, and submission to the Quality Control Process
  • Provides response on supply requests, corrections, patient reports, and other inquiries and concerns. Requests project management assistance, when necessary.
  • Documents meeting minutes & maintains the Project Dashboard Tracker spreadsheet and allows for edits from the Project Manager to be provided and distributed to attendees within 24–48 hours.
  • Addresses escalated 4th day site queries & Double Data Entry quires through communication with the investigator site, sponsor, & PM contacts.
  • Manages Study Closure Protocol notes as needed in applicable database.
  • Completes and Submits Work Order requests to our Clinical Trial Materials department as requested.
  • Provides study‑specific (non‑client facing) management reports to clients on a reoccurring basis.
  • Facilitates distribution of study documents, such as the distribution of site memos to sites and sponsors, at the request of Project Managers.
  • Manages Portal User Account Access in applicable system, including but not limited to creating, adjusting, and deactivating user’s access.
  • Supports Study Set Up Managers with study set up tasks that include but are not limited to:
    • Creation of Sales Force Projects, Updating Sales Force tasks/milestones/project health/Opportunity Amendments
    • Creation of study specific email addresses.
    • Creation of study in Replicon
  • Exhibits an understanding of each protocol from a Project Coordinator’s perspective.
  • Serves as a reference point for clinical investigators, handling questions, concerns, and complaints.
  • Performs other related duties and tasks as necessary or as assigned.
Education and Experience

Required: We’re looking for someone who shines in customer service, stays organized, communicates well, juggles multiple tasks with ease, and connects naturally with others.

Preferred…
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