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.
V&I Outcomes Project Manager
Description of Roles and Responsibilities
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Provides support for key real-world evidence (RWE) processes and quality and compliance activities. Support includes the planning, development, execution, and improvement of RWE processes such as the scientific protocol review process and other priority processes and initiatives related to the conduct of real-world evidence, non-interventional research.
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Main responsibilities include general project management support:
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Assist with the development of process specific guidance and training materials
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Manage timely reviews of research documents to ensure high quality, scientifically rigorous research protocols
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Identify and escalate issues related to scope and guidance
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Drive efficiencies for research processes through automation, simplification, and redesign
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Own research related processes and related operational aspects
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Assist with the development of IT systems and solutions
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Track timelines/deliverables and follow up on action items
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Conduct monitoring and tracking of quality deliverables and develop associated metrics
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Develop activity-wide quality metrics, analyze trends, and prepare reports utilizing visualization methods
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Participate in and contribute to project teleconferences
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Liaise with cross functional teams to communicate project status and/or needs
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Participate in process improvement initiatives to ensure research is conducted in an expedient and complaint way
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Must thoroughly understand and describe research related processes, including protocol review process, to internal stakeholders such as Scientists, Study Managers, Quality Assurance, Compliance, IT, and other cross-functional colleagues
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Troubleshoot issues as they arise and work to bring to timely resolution
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May present projects to NIS teams and cross-functional partners
Minimum FTE Years of Experience
Required Experience and Skills:
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Strong project management skills including strong organizational and time management skills
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A background in public health, epidemiologic, clinical and/or outcomes research.
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Proficient with Microsoft office applications and SharePoint
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Strong communication and interpersonal skills
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Ability to be flexible and manage competing deadlines
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Ability to successfully work independently and within a team
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Self-starter, detail and results oriented, able to handle multiple projects simultaneously and comfortable working in a fast-paced environment
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Preferred Experience and Skills:
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Master’s degree in public health or research-related field (such as epidemiology, outcomes research, behavioral sciences, health services research, biological sciences or public administration)
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Experience working on real-world evidence studies and developing protocols
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Experience with the development and maintenance of research-related processes
Educational Requirement
Bachelor's degree required
Preferred Experience and Skills:
• Master’s degree in public health or research-related field (such as epidemiology, outcomes research, behavioral sciences, health services research, biological sciences or public administration)
• Experience working on real-world evidence studies and developing protocols
• Experience with the development and maintenance of research-related processes
Location
US
FTE (Days/Month)
Standard working days
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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 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.
