Clinical Trials Project Manager

Rochester Regional Health

. 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, including protocol development, regulatory compliance, and client communication. Proficient in project management and quality assurance within clinical laboratory settings.

Highest-signal resume keywords

Project Management ExperienceClinical Trial ManagementRegulatory Compliance KnowledgeProblem Solving SkillsCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Protocol ReviewGlobal Laboratory Specification Document DevelopmentQuality Audit ParticipationProject Budget EvaluationProtocol-Specific Procedure Development

Soft Skills

Client LiaisonTroubleshootingTraining FacilitationConfidentiality Maintenance

Industry Keywords

FDA RegulationsGCPICHNYSDOHClinical Trials

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 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
Manage 10 to 25 protocols after the training period
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 review project budgets
Conduct investigator training sessions by telephone or at investigator meetings
Travel to client events and ACM international locations
Ensure client goals and timelines are met; troubleshoot and resolve problems
Perform assigned on-call coverage duties
Manage regulatory study documentation, including collection, maintenance, and archiving
Develop protocol-specific procedures as needed
Follow applicable company policies, procedures, and regulatory requirements

Requirements

What you’ll need

1+ years project management experience
Experience working in a clinical trial, laboratory or healthcare setting
Excellent problem solving and communication skills
General working knowledge of FDA, NYSDOH, GCP, ICH and other pertinent regulations as they pertain to central laboratory functions
Ability to travel overnight, including frequent weekend travel
Passport qualifications for international travel
Ability to take assigned on-call coverage duties
Ability to maintain patient and client confidentiality
Ability to perform sedentary, office-based work with prolonged sitting and minimal lifting
Bachelor's Degree is preferred, not required

Benefits

Comp & perks

Full-time employment
40 hours per week, Monday–Friday daytime schedule
Additional pay components may be eligible
Travel to client events and ACM international locations
Equal opportunity employment