Clinical Trials Associate Project Manager

ACM Global Laboratories

. Liaise with ACM Global Central Laboratory clients and represent laboratory aspects of clinical trials .

Posted 10/16/2026full-timeRemote • United StatesJuniorMid-Level💰 $65,000 - $85,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, including protocol review, regulatory documentation, and quality audits. Proficient in client communication and project management within a laboratory or healthcare setting.

Highest-signal resume keywords

Clinical Trials ManagementProtocol ReviewRegulatory DocumentationQuality Audits SupportClient Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Protocol SetupGlobal Laboratory Specification DocumentsInvestigator Manuals DevelopmentProject Metrics AnalysisBudget ReviewRegulatory ComplianceStudy Documentation ManagementTroubleshootingProblem-Solving

Soft Skills

Communication SkillsCustomer Satisfaction MaintenanceConfidentiality Maintenance

Certifications & Qualifications

Associate's Degree Preferred

Industry Keywords

FDA RegulationsNYSDOHGCPICHClinical TrialsLaboratory Functions

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Liaise with ACM Global Central Laboratory clients and represent laboratory aspects of clinical trials
Coordinate assigned clinical trials from setup through maintenance and study closeout
Serve as ACM’s primary client point of contact and maintain customer satisfaction
Manage low-complexity studies and varying numbers of protocols
Review clinical protocols and assist with protocol setup
Develop or support Global Laboratory Specification Documents, Investigator Manuals, and protocol-specific Global Work Practice Instructions
Participate in and support clinical-trial quality audits and inspections
Evaluate and communicate monthly project metrics and analyze trial activity, including monthly budget review
Ensure study goals and timelines are met; troubleshoot and resolve problems
Provide assigned on-call coverage
Manage regulatory-required study documentation in accordance with regulations, company policies, and client contracts
Develop protocol-specific procedures as needed
Provide project-management administrative support and perform other assigned duties

Requirements

What you’ll need

Minimum of 1 year of experience working in a clinical trials, laboratory or health care setting required
General working knowledge of FDA, NYSDOH, GCP, ICH and other pertinent regulations as pertains to central laboratory functions
Ability to manage low complexity studies with varying numbers of protocols
Experience reviewing clinical protocols and supporting protocol set-up functions
Ability to develop or support Global Laboratory Specification Documents, Investigator Manuals, and protocol-specific Global Work Practice Instructions
Ability to support quality audits and inspections of clinical trials
Knowledge of regulatory study documentation, collection, maintenance, and archiving requirements
Excellent problem-solving and communication skills
Ability to maintain patient and client confidentiality
Associate’s degree strongly preferred