Associate Clinical Project Manager, Sponsor Dedicated

IQVIA

Associate Clinical Project Manager providing oversight of clinical trials with IQVIA, ensuring data quality and regulatory compliance for efficient study execution.

Posted 5/12/2026full-timeRemote • New Jersey, Pennsylvania • 🇺🇸 United StatesJuniorMid-Level💰 $68,400 - $232,800 per yearWebsite

About the role

Key responsibilities & impact

Provide country-level oversight of clinical trials from start-up through closeout
Ensure high-quality data delivery and regulatory compliance
Collaborate closely with cross-functional teams
Manage site selection and patient recruitment strategies
Support project execution and maintain inspection readiness
Drive risk-based mitigation plans and resolve study challenges

Requirements

What you’ll need

Bachelor's Degree In life sciences or related field required
3 years clinical trial management experience
Intermediate level knowledge of principles, theories, and concepts of a job area
Knowledge of clinical trials and regulatory requirements
Strong written and verbal communication skills
Strong presentation skills
Strong problem solving skills
Planning, time management and prioritization skills
Good software and computer skills, including MS Office applications

Benefits

Comp & perks

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial managementdata deliveryregulatory compliancesite selectionpatient recruitment strategiesrisk-based mitigationproblem solvingplanningtime managementprioritization

Soft Skills

written communicationverbal communicationpresentation skillscollaborationorganizational skills