Clinical Project Manager

Description:

As a Clinical Project Manager, you will oversee and lead the execution of clinical trials from start to finish, ensuring the successful delivery of projects while maintaining high-quality standards and adhering to timelines and budgets.

This role would be suitable for an experienced CPM from a CRO or Pharma setting, with experience leading early-phase clinical trials.

Responsibilities
 

• Lead and manage the entire lifecycle of clinical trials, ensuring compliance with protocols, regulatory requirements, and quality standards.
• Develop and oversee project timelines, budgets, and resource allocation.
• Collaborate closely with cross-functional teams, including clinical operations, data management, and regulatory affairs.
• Monitor trial progress, identify potential risks, and implement mitigation strategies to ensure successful trial outcomes.
• Serve as the primary point of contact for clients, providing regular updates and addressing any project-related queries or concerns.
   

Requirements
 

• Proven experience as a Clinical Project Manager within the CRO or pharmaceutical industry.
• In-depth knowledge of clinical trial processes, regulations (e.g., ICH-GCP), and best practices.
• Strong project management skills, including the ability to handle multiple projects simultaneously.
• Excellent communication, leadership, and problem-solving abilities.
• Proficiency in using project management tools/software.
• [Optional] Relevant certifications (e.g., PMP, CCRA) are a plus.