Clinical Research Associate I

As a Clinical Research Associate I 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 Barcelona, Spain
You will:
Conduct and report all types of onsite monitoring visits.
Be involved in study startup.
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.
College/University degree in Life Sciences.
Minimum of 1 year of experience as a Study Coordinator, or
At least 6 months of experience as a Clinical Research Associate.
Full working proficiency in English and Spanish.
Fluent in Catalan.
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.

Employment type
Full-time

Work arrangement
No