Senior Clinical Research Associate

Established in 1997, COMAC MEDICAL is a trusted, forward-thinking CRO delivering innovative, tailored solutions to the pharmaceutical and biotechnology industries. With a strong footprint across Europe and a team of 250+ talented professionals, we take pride in our commitment to quality, agility, and scientific excellence throughout every phase of clinical development.

We are looking to hire an experienced Senior Clinical Research Associate to join our clinical monitoring team.

Your Mission

You will be a key driver of successful clinical trial execution by ensuring high-quality site conduct and a positive investigator experience.

Your role includes:

• Leading feasibility assessments and site qualification activities
• Building strong, collaborative relationships with investigators and site personnel
• Developing robust knowledge of study protocols and operational procedures
• Supporting essential documentation (protocols, CRFs, regulatory files)
• Conducting on-site and remote monitoring to uphold compliance and patient safety
• Overseeing recruitment, retention, deviations, and inspection readiness
• Proactively identifying and resolving performance or quality concerns
• Partnering closely with study leadership to escalate and manage issues
• Contributing to Investigator Meetings and study-related events

What You Bring

You are a confident communicator and trusted partner to clinical sites, with:

• Bachelor’s or Master’s degree in Life Sciences (Biology, Pharmacy, Chemistry, etc.)
• Minimum 3 years of independent monitoring experience as a CRA
• Strong grasp of ICH-GCP, clinical operations, and local regulatory standards
• Excellent planning, prioritization, and relationship-building skills
• Analytical mindset with the ability to troubleshoot challenges effectively
• Proactive outlook and accountability in a fast-moving environment
• Readiness to travel (up to 30%)
• Professional fluency in English and proficiency with MS Office tools

Why Join COMAC MEDICAL?

Because here, your work matters - and your growth does too.

• Be part of a motivated, supportive, and internationally diverse team
• Work on complex, multi-phase studies across multiple therapeutic areas
• Unlock continuous development and clear career progression pathways
• Contribute to a proven high-performance organization known for: Advanced Phase I expertise; Exceptional quality and on-time delivery; Full-service global solutions

Take the Next Step in Your CRA Career

If you’re ready to bring your expertise to a leading CRO that values innovation and people, we’d love to hear from you.

Please send your CV in English. Only shortlisted candidates will be contacted.