Site Monitoring Lead (FSP) Inflammation Trials
Primary Location: Germany, Remote Job ID R0000036495 Category Clinical Trials Date Posted 11/04/2025Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Flexible
- Organized
- Problem-solver
- Self-starter
About This Role
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 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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Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
- APEX CRA
- CRA I
- CRA II
- Senior CRA
- Project ManagementSubject Matter ExpertPeople Management
Employee Insights
TEAM IMPRESSIONS
Why Clinical Research Associates work at Parexel
