IQVIA · 22 hours ago
Associate Clinical Project Management Director, Cross TA
Philadelphia, PA
Full-time
Hybrid
Director/Executive
$93K/yr - $286K/yr
8+ years expIQVIA is a leading global provider of clinical research services and healthcare intelligence. They are seeking an experienced Associate Clinical Project Management Director to lead and coordinate clinical trial management activities, ensuring successful planning, execution, and closure of trials while interfacing with various stakeholders.
AnalyticsHealth CareLife Science
Responsibilities
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
Escalate and resolve trial issues and contribute to CAPA processes
Support site selection and feasibility assessments
Monitor enrollment commitments and ensure recruitment plans are in place
Oversee selected vendors and review related deliverables and invoices
Coordinate with vendors such as IVRS, Central Labs, ePRO, Imaging, Translation, and Ancillary Supplies
Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans)
Ensure timely filing, archiving, and retention of trial documents
Provide central documents for regulatory submissions
Support Health Authority inspections and internal audits
Develop and deliver trial-specific training materials
Coordinate and participate in Investigator Meetings
Establish country budgets and monitor actuals vs. forecast
Understand Out-of-Pocket (OOP) and FTE cost drivers
Qualification
Required
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
Excellent communication, decision-making, and analytical skills
Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems
Experience in virtual team coordination and stakeholder engagement
Ability to manage ambiguity and drive solutions proactively
Preferred
Monitoring or data management experience
Experience in budget planning and financial oversight
Ability to mentor junior CTMs and lead special initiatives or task forces
Therapeutic area expertise and ability to act as protocol expert
Benefits
Incentive plans
Bonuses
Health and welfare and/or other benefits
Company
IQVIA
IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
10001+ employees
H1B Sponsorship
IQVIA has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (294)
2023 (261)
2022 (229)
2021 (208)
2020 (180)
Funding
Current Stage
Public CompanyTotal Funding
$3.5B2025-06-02Post Ipo Debt· $2B
2023-11-14Post Ipo Debt· $500M
2023-05-18Post Ipo Debt· $1B
Leadership Team
Chris Colapietro
Vice President, Customer Engagement
Jonathan Morris
VP & GM US Healthcare
Recent News
Sabin Vaccine Institute
2025-12-04
Company data provided by crunchbase