Develop and manage clinical project plans and timelines to identify and complete clinical trial milestones with accountability for successful completion of all project deliverables in accordance with GCP, all applicable regulations, and SOPs.
Serve as the primary lead of assigned clinical trial(s)
Provide direction, guidance, and oversight of clinical core teams to execute projects and initiatives
Manage project status and appropriate communication both internally and externally
Analyze trial performance to plan and develop corrective actions.
Identify and communicate study risks, recommend and lead in the implementation of mitigation strategies in collaboration with management
Oversee the selection of study sites and clinical vendors
Provide mentoring and coaching to other project team members
Requirements
Bachelor's degree in related field with 8 years of previous experience required or equivalent work experience based on Edwards criteria
Previous clinical research trial experience managing complex clinical studies
Ability to travel up to 30% to Irvine, CA, Headquarter
Benefits
Competitive salaries
Performance-based incentives
Wide variety of benefits programs to address diverse individual needs
Applicant Tracking System Keywords
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