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.