Top Remote Pharmaceutical Project Management Jobs

Conduct audits to ensure compliance with ISO standards, develop audit plans, assess client facilities, and identify areas for improvement while maintaining positive client relationships.

The Clinical Project Manager leads cross-functional teams to oversee and deliver clinical trials, managing project timelines and stakeholder communications while ensuring regulatory compliance and quality standards are met.

The IRT Manager oversees the IRT systems in oncology studies, manages vendor relationships, ensures compliance, and collaborates with multiple departments to ensure efficient operations.

Oversee the planning, execution, and close-out of clinical research studies ensuring regulatory compliance and timely milestones while leading cross-functional teams and managing sponsor relationships.

The Associate Director - Global Regulatory Policy & Strategy will support U.S. regulatory policy campaigns, develop Lilly policy positions, and engage with external stakeholders to effect policy change improving drug development efficiency.

The Project Manager oversees clinical trials, managing their coordination, and ensuring all deliverables meet customer expectations with a focus on quality and efficiency.

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

The End-to-End Program Lead is responsible for overseeing the design, construction, and commissioning of new facilities, ensuring project goals are met within budget and timelines, while managing a high-performance team.

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.

Lead country/regional study operations from startup through close, overseeing CROs and site activation, managing timelines, budgets, risks, recruitment, vendor deliverables, and resolving escalations to ensure timely study delivery and compliance.