Clinical Project Manager - Remote

Overview

Celerion is looking for a Clinical Project Manager who will be responsible for the independent management of multi-center site activities ensuring compliance to protocol, ICH Good Clinical Practices, Standard Operating Procedures and regulatory and local requirements.

In Short

• Lead initiation, maintenance and close out activities of multi-center studies.
• Ensure compliance with protocols and regulatory requirements.
• Plan and procure team resources for study activities.
• Develop and oversee study plans including project management and risk management.
• Coordinate activities with laboratories and external service providers.
• Review and negotiate site budgets and contracts.
• Maintain effective communication with sponsors and internal departments.
• Travel roughly 30% primarily in the US.
• Flexible schedule is important due to international footprint.

Requirements

• Bachelor's degree required, preferably in science or nursing.
• Clinical research experience as a CRA or Research Coordinator preferred.
• Experience in business development processes.
• Ability to work across multiple projects.
• Experience with renal and hepatic impairment studies is an asset.
• Willingness to travel up to 30% (regional).
• Excellent problem-solving and decision-making skills.

Benefits

• Opportunity to work in a dynamic clinical research environment.
• Home-based position with flexible scheduling.
• Engagement in innovative drug development processes.