Clinical Research Associate

As a Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Office-Based in Sofia, Bulgaria

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (if applicable)
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions


• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in Bulgaria
• Experience in all types of monitoring visits in Phase II and/or III
• Full working proficiency in English and Bulgarian
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel
• Valid driver’s license (if applicable)

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

If interested, apply via