PpAbbVie'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. For more information about AbbVie, please visit us at. Follow @abbvie onLinkedIn, Facebook ,Instagram ,X andYouTube. /p h3Job Description /h3 pThe 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. /p h3Responsibilities /h3 ul liDefines and drives the operational strategies and deliverables for one or more clinical studies /li liResponsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures) /li liProactively manages budget, timelines and study issues; brings scientific acumen, technical expertise and global mindset to drive achievement of study objectives /li liLeader of the cross functional Clinical Study Team /li liLeads clinical operations planning through to execution via cross functional matrix environment and influences cross functional stakeholders to drive milestone achievement /li liEffectively manages vendors and a diverse set of external stakeholders including site staff, Key Opinion Leaders and patient groups /li liBrings a growth mindset, demonstrated by a willingness to continuously learn, grow and adapt, give and receive feedback, see challenges as opportunities /li liCoaches and effectively supports cross functional team members, delegates and empowers to the right level, actively contributes to Development Operations community /li liContributes towards operational efficiencies and brings innovative ideas to their teams and studies /li liDemonstrates excellent communication and problem solving skills /li liPuts patients and customers at the center of what we do /li liNavigates ambiguity and thrives even when not having all the information /li liOn a given study responsible for (but not limited to): ul lithe development of the clinical study design and associated systems, tools and documents /li listudy budget creation and oversight /li livendor selection, scope development, management and oversight of external vendors /li liproactively identifying risks and addressing and/or escalating study related issues and opportunities for efficiency /li liempowered decision maker on operational aspects of study execution /li /ul /li liCreates an inclusive and innovative environment where staff and studies/programs will succeed /li liProvides leadership to Study Management Associates – lead, delegate and support activities to deliver on study milestones /li /ul h3Qualifications /h3 ul liBachelor’s Degree or equivalent degree is required /li li6 years of demonstrated pharma-related and/or clinical research related experience or equivalent required /li liPreferred exposure in study initiation through study completion in Phase 1-4 and/or Medical Device Trial Experience /li /ul h3Additional Information /h3 pAbbVie 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. /p pUS Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: /p /p #J-18808-Ljbffr