As a (Senior) 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.
You will :
Conduct and report all types of onsite monitoring visits
Perform CRF review, source document verification and query resolution
Be responsible for site communication and management
Supervise study activities, timelines, and schedules on the country level
Be a point of contact for in-house support services and vendors
Be involved in quality control, such as compliance monitoring and reports review
Participate in feasibility research
College / University degree in Life Sciences or an equivalent combination of education, training & experience
Sufficient experience of independent on-site monitoring
Experience in all types of monitoring visits in Phase II and / or III
Experience in Oncology / Hematology / Infectious Disease / GI therapeutic areas
Full working proficiency in English and Greek
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
Advance your career in clinical research and lead challenging full-service projects on the country / regional level while growing with a rapid company, that puts its people first! You will get hands-on involvement in every aspect of the study.
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
We offer :
Extensive training and friendly, collegial team
Competitive salary and benefits package
Opportunities for personal and professional growth