Supplier Performance Management Monitor
United States of America, Remote Job ID R0000033323 Category Project Leadership Date Posted 04/30/2025Overview
As a part of the global Project Leadership group at Parexel, you are responsible for leading cross-functional teams to deliver high-quality and patient-focused clinical trials and help bring life-changing treatments to market faster. You collaborate with clients and internal stakeholders to identify project requirements, develop project plans, and manage project timelines and budgets. The role requires strong leadership and communication skills, the ability to work under pressure, and a passion for improving patients' lives.
In return, Parexel offers a supportive work environment, and a high degree of empowerment and accountability to lead your studies. Within this role, you work with a diverse set of clients and therapeutic areas, and you are encouraged to take on new challenges and pursue your interests.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Adaptable
- Communicator
- Collaborative
- Leadership
- Proactive
- Problem-solver
About This Role
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
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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Potential Career Path
Parexel offers a growth path with diverse therapeutic areas and clients, so you can grow according to your interests.
- Associate Project Leader
- Project Leader
- Senior Project Leader
- Associate Project Director
- Project Director
- Director, Project Leadership
- Senior Director, Project Leadership
Employee Insights
Why Project Leaders work at Parexel
