Clinical Program Manager

Job Summary

To support the execution of regional and global clinical studies in orthopedic devices and biologics, the full-time Clinical Program Manager will plan, initiate, and manage projects, ensuring compliance with regulatory requirements while collaborating with internal stakeholders and external vendors in a remote environment.

Key Responsibilities:

• Establish study/project team goals and lead all phases of assigned studies/projects to ensure compliance with SOPs and regulatory guidelines
• Provide accurate study/project information and metrics to management, proactively identifying and resolving issues during study conduct
• Oversee the financial life cycle of study execution, including site budgets and forecasting, while tracking key study metrics using relevant tools

Required Qualifications:

• BA/BS degree in Life Sciences or related field; Master's level education preferred
• Minimum 8 years of clinical trial experience, with at least 2 years in a people management role
• Strong knowledge of ICH/GCP and relevant 21 CFR requirements
• Experience in clinical study design, planning, and management, preferably in the medical device sector
• Proven effective leadership skills and ability to thrive in a fast-paced, entrepreneurial environment