Study Project Manager I

The Study Project Manager I drives the connection between science and operational delivery and ensures operational excellence in planning and execution of clinical research studies across all development stages. The Study Project Manager I is responsible for and ensures clinical research studies are executed with quality and efficiency on-time within budget and meet company objectives. The Study Project Manager I achieves these objectives by bringing scientific acumen strategic thinking innovation experience in clinical study operations management and stakeholder management to address risks and challenges. The Study Project Manager I serves as leader of one or more cross functional Clinical Study Teams leading clinical operations from planning through to execution in a cross functional matrix environment.

Responsibilities

• -Defines and drives the operational strategies and deliverables for one or more clinical studies
  -Responsible for executing clinical studies in compliance with quality standards (ICH/GCP Global Regulations and AbbVie policies and procedures).
  -Proactively manages budget timelines and study issues; brings scientific acumen technical expertise and global mindset to drive achievement of study objectives
  -Leader of the cross functional Clinical Study Team
• -Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement
  -Effectively manages vendors and a diverse set of external stakeholders including site staff Key Opinion Leaders and patient groups
  -Brings a growth mindset demonstrated by a willingness to continuously learn grow and adapt give and receive feedback see challenges as opportunities
• -Coaches and effectively supports cross functional team members delegates and empowers to the right level actively contributes to Development Operations community
  -Contributes towards operational efficiencies and brings innovative ideas to their teams and studies
  -Demonstrates excellent communication and problem solving skills
  -Puts patients and customers at the center of what we do
  -Navigates ambiguity and thrives even when not having all the information
• On a given study responsible for (but not limited to) :
  - the development of the clinical study design and associated systems tools and documents
  - study budget creation and oversight
  - vendor selection scope development management and oversight of external vendors
  - Proactively identifying risks and address and/or escalate study related issues and opportunities for efficiency
  - Empowered decision maker on operational aspects of study execution.
• - creating an inclusive and innovative environment where staff and studies/programs will succeed
• Provide leadership to Study Management Associates lead delegate and support activities to deliver on study milestones

Qualifications :

• Bachelors Degree or equivalent degree is required
• 6 years of demonstrated pharma-related and/or clinical research related experience or equivalent required.
• Preferred exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time