Study Project Manager, II - Hybrid

Study Project Manager II AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. The Study Project Manager II drives the connection between the asset and operational delivery and execution of one or more clinical research studies. Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II achieves these objectives by bringing scientific acumen, strategic asset level thinking, innovation, expertise in clinical study operations management and stakeholder management to address risks and challenges. Responsibilities: Defines and drives the study level operational strategies and deliverables – linking these to asset level goals Brings strategic, asset level thinking and innovative problem solving to study planning and execution Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures). Effectively present and contribute to discussions on study operations at asset level strategic meetings Leads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement Demonstrates the skills, experience and critical thinking to lead cross functional teams with minimal supervision. Expertise in end-to-end clinical study operations management (all phases, set up to close out) Coaches and mentors team members, delegates and empowers to the right level, actively contributes to Development Operations community Demonstrates leadership with high level cross functional stakeholder management and influencing skills Lead operational efficiencies and foster a culture of innovation 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. Qualifications: Bachelor's Degree or equivalent degree is required, 8 years of demonstrated pharma-related and/or clinical research related experience or equivalent required. Preferred Oncology Clinical Trial Experience Preferred exposure in study initiation through study completion in Phase 1-4 and/or Clinical Trial Experience Additional Information: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs. 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 US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: Recruitment Fraud Alert AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process. If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks. If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately. Protect yourself by verifying job offers and communications. Your safety is important to us. Yes, 10% of the Time Pay Range: $124500 - 236500 USD Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role. AbbVie