Top Remote Biotech Project Management Jobs

The Manager, Site Resourcing will oversee site management for clinical research, coordinate teams and budget, and ensure compliance with regulations.

The Director, Global Regulatory Project Management leads oncology regulatory strategies, ensuring successful global drug submissions, while driving operational excellence and collaboration across teams.

The Associate Director is responsible for leading global regulatory project management, ensuring successful regulatory submissions, and facilitating cross-functional collaboration to maintain product market access worldwide.

The Director of Global Regulatory Project Management leads oncology regulatory strategies, ensures timely submissions, manages global project teams, and fosters cross-regional collaboration to maintain market access for products.

Manage and oversee clinical studies for aortic arch repair technologies, ensuring compliance with regulatory requirements and effective project management through collaboration with stakeholders.

The Senior CRA 2 is responsible for site monitoring, site management, ensuring compliance with regulatory requirements, managing study activities, and leading clinical trials for the company.

The Transformation Leader drives Lean principles and enterprise-wide transformation at GE HealthCare, enhancing agility, reducing waste, and improving customer responsiveness through strategic initiatives and cross-functional collaboration.

Coordinate and execute internal Global Marketing and Market Access projects, manage AP/travel/legal/procurement functions, maintain reports and KPIs, oversee communications channels, and develop strategic content with subject matter experts.

The Senior Global Trial Manager oversees clinical trials globally, ensuring compliance and progress according to regulations and protocols.

The Senior Clinical Project Manager will lead Phase III oncology and hematology trials, managing projects and cross-functional teams while ensuring timely and quality delivery.

The Study Start Up Oversight Lead accelerates site activations, ensures compliance in clinical studies, oversees timelines, and drives process improvements.

Lead end-to-end management of diverse events, including planning, execution, and budget management, while establishing relationships with internal customers.