A globally recognized Contract Research Organization (CRO), specializing in comprehensive drug discovery, development, and manufacturing services, is seeking an experienced Senior Clinical Project Manager. This organization, known for its innovative approach and global impact in medical research, offers a unique opportunity to lead and manage pivotal clinical projects on an international scale.
As a Senior Clinical Project Manager, you will play a crucial role in overseeing, coordinating, and executing large-scale clinical projects. This position requires a strategic, detail-oriented individual capable of working collaboratively across various functions and ensuring the successful completion of complex clinical trials.
The position is a remote role which can be conducted from anywhere in US. Applicants must already have the right to work in the US to be considered for the position.
Lead project teams, ensuring successful contract reviews, resource applications, and team training.
Develop and maintain project documentation, including SOPs and risk management plans.
Monitor project timelines, budgets, and adherence to international regulations and protocols.
Report and manage safety events and trial deviations in compliance with regulatory requirements.
Collaborate with Data Managers on trial design and oversee site monitoring.
Manage and optimize project resources, maintaining high standards of quality and revenue.
Advanced degree in Medicine, Pharmacy, Life Science, or a related field.
Strong knowledge of ICH-GCP, Chinese GCP, and relevant regulatory standards.
At least 10 years of experience in clinical trials, with a minimum of 8 years in clinical trial management.
Proven experience in phase I/II/III clinical trial management, preferably within a CRO environment.
Demonstrated skills in revenue and cost management in clinical projects.
We invite dedicated Clinical Project Managers seeking to make a significant impact in global clinical research to apply for this role. For similar positions across clinical project management or the wider pharmaceutical lifecycle, feel free to reach out directly.