Site Monitoring Lead

2 days ago

Germany Germany, India PAREXEL International Ltd Full time € 60,000 - € 90,000 per year
Job Description

Parexel FSP has a new opening within our FSP Clinical Operations Team in Germany for a Site Monitoring Lead.

This role 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 decisions 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.

#LI-TA1

#LI-REMOTE

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