Job Title: CRA II – Germany (Remote)
Position Type: Permanent
Location: Remote Germany
About Our Client
Our client is a well-established organisation within the clinical research sector, supporting pharmaceutical and biotech partners with high-quality clinical trial services. Working across regulated environments, our client’s team focuses on rigorous study conduct, patient safety, and reliable data, enabling sponsors to progress important therapies through the development pipeline.
As part of a growing clinical research function, you will be joining a supportive environment where collaboration, professional integrity, and continuous learning are valued.
Role Overview
As a Clinical Research Associate II, you will play a key role in the monitoring and oversight of clinical studies conducted in Germany. This is a permanent, remote position, offering you the flexibility to work from home while remaining closely connected to our client’s team and trial sites. You will use your experience in clinical research and as a Clinical Research Associate to ensure trials are conducted in line with protocols, regulatory requirements, and quality standards.
This role is well suited to a CRA who is ready to take ownership of site-level activities, build strong relationships with investigators and site staff, and contribute to the reliable delivery of clinical data.
Key Responsibilities
• Perform on-site and remote monitoring activities for clinical research studies in Germany, in line with protocol, GCP, and applicable regulations.
• Conduct site initiation, routine monitoring, and close-out visits, ensuring all trial activities are appropriately documented.
• Review source data and verify case report forms for accuracy, completeness, and adherence to the study protocol.
• Support site staff in understanding and implementing study requirements, providing guidance on procedures and documentation.
• Identify, document, and follow up on site issues, deviations, and action items until resolution.
• Maintain regular communication with investigators and site teams to foster strong working relationships and encourage patient recruitment and retention.
• Collaborate with our client’s team to share site insights, contribute to risk assessments, and support study timelines.
• Prepare and submit timely, accurate monitoring reports and other required study documentation.
About You
• Experienced in Clinical Research and currently working as a Clinical Research Associate with independent on-site monitoring on global studies
• Comfortable operating in a hybrid or remote set-up while maintaining strong engagement with sites and colleagues.
• Able to work independently, organise your monitoring responsibilities, and manage multiple priorities.
• Detail-focused, with a commitment to data quality, patient safety, and regulatory compliance.
• Skilled in building collaborative relationships with investigators, site staff, and internal teams.
What This Role Offers
• The opportunity to contribute to meaningful clinical research within an established clinical research sector organisation and exposure to new scientific research in the world of rare disease, oncology and a variety of other therapeutic areas.
• Daily collaboration with our client’s team, providing exposure to a range of studies and operational approaches.
• A role that supports continued professional growth in monitoring, site management, and clinical operations.
How to Apply
If you are an experienced Clinical Research Associate looking to take the next step in your career as a CRA II in Germany, we would like to hear from you. Please submit your CV, and we will be in touch to discuss this opportunity with our client’s team in more detail.