Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
1A
150 Altasciences Clinical Kansas Inc
Project Coordinator
Entry-Level JobVerifiedNo experience needed
Career Insights for Project Coordinator
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Kansas data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Project Coordinator coordinates project team work on projects with a defined scope, start and completion point, and assists the project manager. Coordinates project team activities and communication. Organizes meetings and tracks project budgets and schedules. Organizes contracts, files and reports. May coordinate projects in construction, information technology or in other industries.
$60,138 / year median in Kansas
+6% projected growth
Job Description
About The Role The Project Coordinator supports the end-to-end execution of clinical trials by coordinating study activities, evaluating study information, tracking risks, maintaining inspection-ready documentation, and exercising judgment to prioritize actions, identify issues requiring escalation, and support timely decision-making in collaboration with the Project Manager (PM), study team, sponsors, vendors, and internal stakeholders. What You'll Do Here Develop, maintain, and evaluate project-specific timelines in collaboration with the PM to support on-time execution and delivery from project award through archival. Coordinate study-related issues in partnership with the PM, assess urgency and potential impact, and escalate matters appropriately. Maintain effective and timely communication with internal and external stakeholders, including sponsors, clinical sites, vendors, and cross-functional study team members, to support alignment and resolution of outstanding items. Prepare, support, and document internal and external project team meetings, including tracking decisions, action items, follow-ups, and items requiring PM or leadership input. Support the development, review, and maintenance of project-specific documents and plans. Create, maintain, and/or coordinate Trial Master File documentation and related study records to support inspection readiness, including identifying documentation gaps and driving follow-up to resolution. Coordinate with Quality Assurance and project team members to support GxP and regulatory compliance. Coordinate start-up activities with vendors and external sites. Support submissions to institutional review boards and regulatory agencies. Participate in Lessons Learned meetings and contribute observations, process gaps, and improvement recommendations to support department and corporate initiatives. Maintain risk-related trackers or risk register items. Coordinate project-specific training documentation by tracking finalized documents, confirming required training audiences, and escalating missing or delayed training inputs when needed. What You'll Need to