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 to hire a Supplier Performance Management Manager (SPM) ! The SPM manager monitors and drives supplier performance, compliance, and process improvements in clinical trials.
Key Responsibilities:
• Managing and developing individual and supplier-specific objectives
• Coordinating and prioritizing cross-study projects.
• Developing strong global relationships with key functions
• Participating and facilitating of the governance of Technical Service suppliers
• Driving development and review of Independent Review Charters (imaging)
Key Activities:
• Support the development and implementation of standards and processes for evaluation, qualification, selection, management, and monitoring of TSSs
• Support Technical Services staff activities
• Monitor cross-study technical and operational performance of TSS and manage escalated issues to resolution
• Prepare technical training materials for other functions within Amgen
• Participate with Therapeutic Areas and Early Development/Translational Sciences in ongoing work streams and task forces
• Share expertise in emerging technologies through company interactions, literature, and industry conferences
• Contribute to defining department goals
• Contribute to the continuous improvement of Technical Services and the wider Development organization
• Support the integration activities for Amgen acquisitions, as appropriate
Basic Qualifications:
• Doctorate degree
OR
• Master’s degree & 3 years of directly related experience
OR
• Bachelor’s degree & 5 years of directly related experience
OR
• Associate’s degree & 10 years of directly related experience
OR
• High school diploma / GED & 12 years of directly related experience
AND
• Previous direct managerial and/or leadership 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 relevant area (e.g, imaging, laboratory, device technology) and their application to clinical trials
• Management experience of direct reports
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.
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What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
