Senior Clinical Trial Operations Lead (Global)

Atrium Therapeutics; United States; Teletrabalho; USD 171 000 - 189 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Stock options

401(k) with employer match

Wellness program (medical, dental, vis

Unlimited vacation

Resumo da oferta

Atrium Therapeutics is leading in RNA-based therapies for cardiomyopathies and seeks a Senior Clinical Trial Manager to oversee global clinical operations. You will manage CROs, vendors, budgets, and study timelines, ensuring GCP compliance and cross-functional coordination across discovery, development, regulatory, and IT functions.

The role emphasizes rare disease experience, cardiovascular focus, and the ability to navigate complex, multicenter studies with strong leadership and strategic

Qualificações

• Bachelor’s degree in Life Sciences or equivalent field required.
• Minimum 8–10 years of clinical operations experience.
• Experience managing a CRO and complex studies in a leadership role.
• Global Clinical Trial experience in Phase I–III.
• Knowledge of ICH/GCP and regulatory guidelines.

Responsabilidades

• Lead overall clinical study operations, CRO and vendor management, budgets and timelines.
• Provide oversight of CROs, vendors and sites ensuring compliance with GCP and regulatory guidelines.
• Collaborate with clinical development, legal, finance, regulatory affairs, QA and IT.
• Develop study-level timelines, deliverables and KPIs with cross-functional teams.
• Manage investigator selection, drug supply projections, start-up, recruitment and data handling.

Conhecimentos

Project management

Leadership

Communication

Attention to detail

Multi-tasking

Budgeting

Cross-functional collaboration

Risk management

Formação académica

Bachelor’s degree in Life Sciences

Ferramentas

Smart Sheets

MS Excel

Descrição da oferta de emprego

Atrium Therapeutics is leading in RNA-based therapies for cardiomyopathies and seeks a Senior Clinical Trial Manager to oversee global clinical operations. You will manage CROs, vendors, budgets, and study timelines, ensuring GCP compliance and cross-functional coordination across discovery, development, regulatory, and IT functions.

The role emphasizes rare disease experience, cardiovascular focus, and the ability to navigate complex, multicenter studies with strong leadership and strategic