Clinical Trials Project Manager

ACM Global Laboratories

. Liaise with ACM Global Central Laboratory clients as the laboratory representative for clinical trials .

Posted 9/24/2026full-timeRemote • New York • United StatesJunior💰 $80,000 - $100,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, ensuring compliance with regulatory standards, and maintaining client satisfaction. Proficient in developing documentation and conducting training while effectively analyzing project metrics.

Highest-signal resume keywords

Project Management ExperienceClinical Trial ManagementRegulatory Knowledge (FDA, GCP, ICH)Client Liaison SkillsProtocol Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementProtocol DevelopmentProject Metrics AnalysisQuality Audits ParticipationRegulatory Documentation Maintenance

Soft Skills

Problem SolvingCommunication SkillsCustomer Satisfaction Focus

Certifications & Qualifications

Bachelor's Degree

Industry Keywords

Clinical TrialsLaboratory FunctionsPatient ConfidentialityOn-Call CoverageInvestigator Training

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Liaise with ACM Global Central Laboratory clients as the laboratory representative for clinical trials
Liaise internally with all groups to ensure trials follow the Global Laboratory Specification Document
Manage assigned clinical trials from setup through maintenance and study closeout
Serve as the client's primary point of contact and maintain customer satisfaction
After training, manage 10 to 25 protocols depending on scope and complexity
Review clinical protocols and assist with protocol setup
Develop Global Laboratory Specification Documents, Investigator Manuals, and protocol-specific Global Work Practice Instructions
Participate in and document clinical trial quality audits and inspections
Evaluate and communicate monthly project metrics and analyze trial activity, including monthly budget review
Conduct investigator training sessions by telephone or at investigator meetings
Travel to client events and ACM international locations as required
Ensure client goals and timelines are met; troubleshoot and solve problems
Provide assigned on-call coverage
Maintain regulatory-required study documentation and archive materials according to regulations, ACM policies, and client contractual clauses
Develop protocol-specific procedures as needed
Follow company policies and procedures while maintaining patient and client confidentiality

Requirements

What you’ll need

1+ years project management experience
Bachelor's Degree is preferred
Experience working in a clinical trial, laboratory or healthcare setting is preferred
General working knowledge of FDA, NYSDOH, GCP, ICH and other pertinent regulations as they pertain to central laboratory functions
Ability to travel overnight, frequently on weekend days
Ability to travel to client events and ACM international locations
Passport qualifications
Ability to take assigned on-call coverage duties
Ability to maintain patient and client confidentiality
Ability to perform sedentary, primarily office-based work with prolonged sitting and minimal physical effort
Excellent problem solving and communication skills are preferred

Benefits

Comp & perks

Overnight travel and travel to client events and ACM international locations
Additional pay components may be available
Potential flexible hours
Reasonable accommodations for reported physical requirements