Site Monitoring Lead (FSP) Inflammation Trials

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds 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 were committed to making a difference.

Parexel 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 industrys 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. bachelors 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. Youll 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 thats shaping the future of clinical research

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