Senior Clinical Trials Project Manager

ACM Global Laboratories

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

Posted 10/16/2026full-timeRemote • New York • United StatesSenior💰 $100,000 - $125,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trial protocols, ensuring compliance with FDA, GCP, and ICH regulations, while effectively communicating with clients and mentoring team members. Proficient in developing laboratory documentation and conducting investigator training to meet project goals and timelines.

Highest-signal resume keywords

Project Management ExperienceClinical Trials ExperienceKnowledge of FDA RegulationsGCP ComplianceProtocol Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementProtocol ReviewBudget EvaluationQuality AuditsRegulatory Documentation Management

Soft Skills

Problem SolvingCommunicationMentoring

Tools & Technologies

Global Laboratory Specification DocumentsInvestigator ManualsGlobal Work Practice Instructions

Certifications & Qualifications

Master's Degree PreferredPassport Qualifications

Industry Keywords

Clinical TrialsHealthcare SettingNYSDOHICHACM Policies

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
Serve as the client’s primary point of contact
Manage 15 to 30 clinical trial protocols after training, including protocols exceeding $6,000,000 in contract value
Oversee regional Project Managers and assigned clinical trial outputs
Mentor junior department and team members
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 study conduct, client goals, and timelines are met; troubleshoot and solve problems
Perform assigned on-call coverage duties
Manage regulatory study documentation and archive materials according to regulations, ACM policies, and client contractual clauses
Develop protocol-specific procedures and contribute to ACM Standard Operating Procedures

Requirements

What you’ll need

3 years project management experience
1 year experience in clinical trials, laboratory or healthcare setting
Working knowledge of FDA, NYSDOH, GCP, ICH and other pertinent regulations as related to central laboratory functions
Ability to manage 15 to 30 protocols after training, depending on scope and complexity
Ability to run protocols regardless of geographic coverage of site selection
Ability to travel overnight to client events and ACM international locations
Passport qualifications
Ability to maintain patient and client confidentiality
Master’s Degree preferred
Excellent problem solving and communication skills preferred

Benefits

Comp & perks

Overnight travel for investigator training sessions, client events, and ACM international locations
On-call coverage duties
Flexible hours may be required
Accommodations considered for reported physical requirements