Senior Clinical Study Manager - Remote-First, Life Sciences

Viz.ai; San Francisco (CA); Híbrido; USD 120 000 - 170 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Remote-first across US & EU

Competitive compensation & benefits

Equity opportunities

Resumo da oferta

Viz.ai is seeking a Senior Clinical Study Manager to lead clinical research trials and pilots for AI-enabled care pathways. You will oversee sponsor oversight of sites, ensure GCP compliance, and partner with Evidence Generation and Product teams to deliver study objectives on time and within budget.

The role emphasizes collaboration across Clinical, Life Sciences, Legal, and Finance functions, with travel up to 30%.

Qualificações

• 6+ years of clinical research experience, preferably in medical device and/or SaaS.
• Bachelor's degree in a scientific discipline or equivalent; other qualifications considered.
• Competent knowledge of clinical study project management practices and terminology.
• Proven ability to lead others to deliver quality results on time, with monitoring and feedback.
• Willing to travel up to 30% as needed.

Responsabilidades

• Oversee start-up, maintenance/operations, and close-out for assigned studies per contract and SOPs.
• Manage operational aspects to ensure data quality and efficient enrollment meeting contractual requirements.
• Lead activities to ensure sponsor oversight of sites per GCP and regulations.
• Collaborate with cross-functional partners to keep studies on schedule and within budget.
• Provide status updates, document study plans, and train colleagues on study management best practices.

Conhecimentos

Clinical research

Project management

Team leadership

Regulatory knowledge

Travel readiness

Formação académica

Bachelor’s degree in science

Ferramentas

GCP knowledge

Descrição da oferta de emprego

Viz.ai is seeking a Senior Clinical Study Manager to lead clinical research trials and pilots for AI-enabled care pathways. You will oversee sponsor oversight of sites, ensure GCP compliance, and partner with Evidence Generation and Product teams to deliver study objectives on time and within budget.

The role emphasizes collaboration across Clinical, Life Sciences, Legal, and Finance functions, with travel up to 30%.