Supplier Performance Management Monitor

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel is looking for a Supplier Performance Management (SPM) Monitor! Key Responsibilities: • Monitoring the collection, processing, and analysis of data by TSS for sponsored clinical trials • Monitoring and evaluating Supplier compliance and data quality • Tracking corrective actions in relation to monitoring issues and audit findings; escalates as appropriate • Developing professional relationships with TSS and with sponsor stakeholders Basic Qualifications: • Doctorate/ Masters/BA/BS/RN/AD/GED • If Master’s degree, 3 years of directly related experience; if Bachelor’s degree, 5 years of directly related experience; if Associate’s degree, 10 years of directly related experience; if GED, 12 years of directly related experience Preferred Qualifications: • 7 years’ work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical, CRO or technical services supplier) • Technologist or work experience in imaging or laboratory technology and their application to clinical trials • Management experience of direct reports Knowledge/Competency: • Technical knowledge of the assigned area of focus (imaging, specialty laboratory testing), including techniques and technologies • Knowledge of Good Clinical Practice (GCP) • QA processes (particularly Corrective and Preventive Action, Deviation Reporting, Auditing) • Exceptional oral and written communication skills • Ability to understand the needs of diverse stakeholder groups • Exceptional problem solving and analytical skills • Ability to define and track metrics • Attention to detail and understanding of the potential impact of clinical data discrepancies • Technical mastery of key sponsor databases and systems #LI-SS1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.