Associate Clinical Project Management Director, Cross TA

IQVIA

Associate Clinical Project Management Director leading and coordinating clinical trial management activities at IQVIA. Supporting trial leaders to ensure compliance, quality, and timely delivery of trial milestones.

Posted 7/7/2026full-timeRemote • Massachusetts, New Jersey, North Carolina, Pennsylvania • 🇺🇸 United StatesLead💰 $93,100 - $285,500 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead the Study Management Team and provide regular updates on trial deliverables.
Ensure real-time tracking and documentation of trial progress.
Maintain inspection-readiness throughout the trial lifecycle.
Act as the primary contact for country and regional staff and internal teams.
Partner with Global Trial Leads to oversee central trial activities from start-up to close-out.
Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans).
Establish country budgets and monitor actuals vs. forecast.

Requirements

What you’ll need

Bachelor’s degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) or equivalent.
Minimum 8 years of experience, with proven leadership in complex trials at a large pharmaceutical company.
Strong knowledge of ICH-GCP and local regulatory requirements.
Proven ability to lead cross-functional teams and manage global trials.
Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems.
Experience in virtual team coordination and stakeholder engagement.

Benefits

Comp & perks

Health insurance
Retirement plans
Flexible work arrangements
Paid time off
Professional development
Bonuses

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Trial ManagementBudget ManagementDocument CreationReal-Time TrackingInspection Readiness

Soft Skills

Team CoordinationCommunication