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SeniorFull-timeGCP
Salary Range
$66,300 - $89,700 /year
This salary is estimated based on similar roles. The actual salary may vary.
About the Role
The Study Project Manager drives the connection between science and operational delivery, ensuring excellence in planning and execution of clinical research studies across all development stages. This role is responsible for executing clinical research studies with quality and efficiency, on-time, within budget, and meeting company objectives.
Key Responsibilities
- →Define and drive operational strategies and deliverables for one or more clinical studies
- →Execute clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures)
- →Proactively manage budget, timelines, and study issues
- →Lead the cross-functional Clinical Study Team
- →Lead clinical operations planning through to execution in a cross-functional matrix environment
- →Manage vendors and external stakeholders including site staff, Key Opinion Leaders, and patient groups
- →Coach and support cross-functional team members
- →Contribute to operational efficiencies and bring innovative ideas
- →Demonstrate excellent communication and problem-solving skills
- →Navigate ambiguity and thrive in challenging situations
Requirements
- ✓Development of clinical study design and associated systems, tools, and documents
- ✓Study budget creation and oversight
- ✓Vendor selection, scope development, management, and oversight
- ✓Proactive identification of risks and addressing study-related issues
- ✓Empowered decision-making on operational aspects of study execution
- ✓Creating an inclusive and innovative environment
- ✓Providing leadership to Study Management Associates
Benefits
- ★Hybrid work model (onsite T-TH)
- ★Opportunities for professional growth and development
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