Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred. Minimum of 3-7 years of clinical research experience or proven competencies for this position. Minimum of 2-4 years of leading a project. Experience managing regional trials (moderate complexity) and/or supportive role in managing complex global trials. Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS. Good communication and interpersonal skills. Good organizational skills, attention to detail, and a customer service demeanor. Demonstrates knowledge of ICH-GCP, relevant Precision SOPs. Working knowledge of project management techniques and tools. Experience working in a cross-functional project management environment. Fundamental understanding of cross-functional management. Fundamental understanding of project planning, risk management and change management. High level of integrity. Ability to lead and inspire excellence within a study team. Ability to create an environment where study team members have a sense of ownership. Results oriented, accountable, motivated and flexible. Good time management, negotiation, critical thinking, decision making, analytical and interpersonal skills. Good presentation, verbal and written communications skills. Fundamental understanding of project management software. Experience in pharmaceutical and/or device research required.