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Leadership
Role Overview:
- Provide leadership, oversight, and mentorship across regional clinical trials.
- Partner closely with Project Managers, Regional Project Leads, and CRAs.
- Focus on remote oversight with minimal travel and few site assignments.
Responsibilities:
- Monitor project timelines, patient enrollment, and data cleaning while ensuring compliance.
- Review monitoring visit reports and manage study risks at site and regional levels.
- Supervise source data verification, ensure data integrity, and coordinate safety information flow.
Qualifications:
- Relevant degree in Life Sciences or equivalent with 4+ years of site monitoring experience.
- Strong experience in Oncology and global clinical projects preferred.
- Full English proficiency and excellent communication and multitasking skills.
Why Join PSI:
- Join a stable, privately held CRO with no mergers or layoffs.
- Enjoy a leadership-focused role with minimal travel.
- Benefit from career development and a collaborative culture.
PSI CRO
PSI CRO is a privately owned, global Contract Research Organization dedicated to advancing medical science and bringing new therapies to patients worldwide. Founded in 1995, the company has over 3,000 employees and prides itself on long-term stability, having never undergone a merger, acquisition, or company-wide layoffs.