Clinical Trial Mid-Level Project Manager

Job Description

Job Description

About Vitalief

Vitalief partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care. Our team combines deep clinical research expertise with results-driven consulting to help organizations operate more efficiently and grow sustainably.

The Role

Vitalief is seeking a highly organized and detail-oriented Mid-Level Project Manager to provide operational oversight and coordination for our client’s Pediatric Acute Leukemia clinical trials. This full-time, fully benefited role serves as the primary liaison between the pharmaceutical clinical research team and CROs, ensuring trials are executed efficiently, on budget, and in compliance with regulatory standards. The Project Manager bridges scientific and operational aspects of clinical research, leading cross-functional teams to deliver high-quality studies evaluating the safety and efficacy of pharmaceuticals.

WHY VITALIEF?

• Contribute to advancing scientific discoveries that improve patient lives.
• PEOPLE FIRST culture with opportunities for growth and innovation.
• Competitive benefits include 20 PTO days + 9 paid holidays; Company-paid life insurance and short / long-term disability; 401(k) retirement program; Comprehensive healthcare plans.
• Salary Range :   $70,000 to $80,000  (commensurate with experience).
• Work Location : 100% Remote  (seeking only candidates that live in the EST Zone).

KEY RESPONSIBILITIES

Trial Planning and Initiation

Trial Execution and Management

Stakeholder Management

Quality and Compliance

QUALIFICATIONS

Education and Experience

PHYSICAL DEMANDS : Prolonged periods sitting working on a computer, standing, walking, visual perception, talking and hearing. Lifting up to 20lbs.

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