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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 Monitoring Lead (FSP) Inflammation Trials
Job ID R0000036495 , GermanyParexel FSP has a new opening within our FSP Clinical Operations Team in Germany for a Site Monitoring Lead.
This roles is dedicated to a single sponsor and will support the Experimental Medicine (Early Clinical Trials) team, focusing on Inflammation studies.
About the Sponsor
Our sponsor is a leading biopharmaceutical company, recognized as one of the industry’s top investors in research and development. With a strong presence in both human and animal health, the company is committed to developing innovative therapies that address areas of high unmet medical need. Founded in Germany in 1885, the organization has remained independent and continues to improve and extend lives worldwide.
About the role:
Lead risk-based site monitoring strategies
Oversee CRO partners to ensure GCP and regulatory compliance
Provide expert guidance to CT Managers and CRAs
Contribute to trial planning, conduct, and close-out
Drive quality, training, and communication across global teams
Knowledge and Experience:
Substantial Site Management or CRA Lead experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Specifically within inflammation trials.
Demonstrated scientific and therapeutic knowledge and operational expertise across all Site Monitoring aspects in clinical trial planning and execution.
Understand dimensions of trial complexity include protocol, patients, sites, countries, vendors.
Ability to prioritize multiple tasks, and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.
Education:
University (e.g., bachelor’s or comparable degree) in life sciences or related field OR several years of equivalent professional education may be acceptable if complemented by solid knowledge in and experience with Site Monitoring and Site Management processes and accountabilities.
Why Join Us?
This is an opportunity to work on cutting-edge early-phase trials with a sponsor that values innovation and collaboration. You’ll be part of a high-performing team making a real impact in areas of unmet medical need.
Apply Today
Take the next step in your career and join a team that’s shaping the future of clinical research
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