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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Site and Monitoring Health Lead - FSP
Job ID R0000042658 , NetherlandsSummary of Key Responsibilities:
Employ risk-based thinking to focus on what is critical to quality, and exhibit an “inspection ready at all times” mentality
Create Study Specific Oversight Plans (SSOP) for aligned trials in scope and/or follow SSOP when conducting oversight activities
Implement various types of oversight encounters and activities as applicable including but not limited to: site risk analysis, site contacts, aggregate review of data, monitoring visit report review, Sponsor Oversight Visits, system/data spot checks, and periodic summaries; ensure timely documentation of these activities is completed and filed
Build relationships with investigators and site staff in region; act as a resource for identifying potential sites for new studies
Utilize root cause analysis to assess identified issues and provide suggested actions to Study Management / CRO to mitigate risk
Support investigator sites less experienced in research; assist in assuring sites are engaged in the study and have what they need to recruit participants successfully
Troubleshoot and use alternative and innovative approaches to solve problems impacting clinical site delivery and quality
Work closely with Clinical Risk & Analytics staff to understand the risk management plan (Risk MAP) for assigned studies, ensure the SSOP is aligned with the Risk MAP, and assess sites who are outliers
Lead oversight and trend meetings with the study team and/or CRO to discuss risks, issues, and trends identified by the SMH team for the trial
Support inspection preparation and management
Maintain awareness of changes in industry and regulatory standards for GCP requirements
Travel on assignment ~ 50% is required. This is a site facing position and travel may fluctuate up or down depending on business need. May include local, regional and international travel.
Requirements
Bachelor's Degree is required. A clinical or advanced degree (RN, MPH, MS, MA, MBA, PharmD,) is preferred
Previous direct monitoring experience gained with a CRO or pharmaceutical company working on multinational clinical studies; Lead CRA/management experience preferred
Experience in all study phases of clinical research (Phase I-III) and experience in both prevalent and rare medical conditions preferred
Previous audit and regulatory inspection experience preferred
Comprehensive and current regulatory knowledge, including GCPs
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