Senior Clinical Research Associate

We are partnering with a leading clinical research organisation to support their search for an experienced Clinical Research Associate (CRA) based in Germany. Our client is a mid‑sized CRO that’s outperforming the market this year through repeat business, multi‑sponsor studies, and a reputation for quality delivery. Working in onsite monitoring, they are offering real progression opportunity in a business that gives back to its team.

It’s a great balance - the scale and stability of a high‑performing CRO, but the autonomy and close‑knit feel of a mid‑sized business.

Key Responsibilities:

• Manage assigned clinical trial sites and act as the primary site contact.
• Conduct site monitoring visits (PSV, SIV, routine monitoring, and close‑out visits).
• Ensure studies are conducted in compliance with protocols, ICH‑GCP, regulatory requirements, and SOPs.
• Support site start‑up activities, including feasibility and site selection.
• Review and maintain essential regulatory documentation.
• Monitor patient enrolment, site performance, and investigational product accountability.
• Provide regular site updates to the project team and contribute to study success.

Requirements:

• Previous clinical research experience, including independent monitoring experience in Germany.
• Strong knowledge of ICH‑GCP and regulatory requirements.
• Fluent in German and English (written and spoken).
• Excellent organisational and communication skills.

What's on Offer:

• Opportunity to join a global and collaborative clinical research environment.
• Strong focus on professional development and career progression.
• Flexible working arrangements and a supportive team culture.
• The chance to contribute to innovative clinical research that improves patient outcomes.
• Incentive bonus schemes that pass the business success directly back to the team.